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Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

11 July 2025

Read the preprint on medRxiv Opens on cambrianbioworks.com

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Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

Diagnostic Utility of Low-Pass Whole Genome Sequencing in Prenatal Detection of Chromosomal Abnormalities in an Indian Cohort

Preprint, not peer reviewed. Low-pass whole genome sequencing of 1,508 prenatal samples from India identified chromosomal abnormalities in 168 cases, a diagnostic yield of 11.1%, with aneuploidies making up 71% of the abnormalities detected.

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