CamSelect Long
CamSelect Long
CamSelect Long
CamSelect Long
CamSelect Long
Increase usable Gb per long-read sequencing flow cell by up to 3x
Increase usable Gb per long-read sequencing flow cell by up to 3x
Increase usable Gb per long-read sequencing flow cell by up to 3x
Increase usable Gb per long-read sequencing flow cell by up to 3x
SKU:
SKU:
SKU:
CBWD018
Pack size:
Pack size:
Pack size:
50 preps
50 preps
50 preps
A new standard for
long-read preparation
Long-read sequencing platforms have finite capacity per run, constrained by pore availability and functional lifetime. In heterogeneous samples, short DNA fragments can generate large volumes of low-information reads while consuming valuable sequencing bandwidth.
CamSelect Long addresses this challenge through tunable cutoff (under 2kb, 5kb, 7kb and 10kb), enriching libraries for longer fragments. This improves the proportion of informative long reads, increases read N50 and pass yield, stabilizes run performance, and enables greater usable data output per flow cell.
Improves read N50 and long-read fraction
Increased usable Gb per flowcell for long read sequencing
Increases pass yield (Q ≥ threshold)
Enhances pore retention and flow-cell efficiency
Low input requirement (≈1 µg DNA)
Automation-ready magnetic bead chemistry
Maximize data yield per read
Maximize data yield per read
Maximize data yield per read
Maximize data yield per read
CamSelect Long improves data yield and N50 while reducing pore consumption, delivering more contiguous assemblies. Libraries were prepared using the Oxford Nanopore technologies (ONT) Native Barcoding Ligation kit (EXP-NBD114) according to manufacturer’s protocol, and sequenced on a PromethION 2 Solo platform with FLO-PRO114M flowcell to a target depth of 5 Gb per sample.
CamSelect Long improves data yield and N50 while reducing pore consumption, delivering more contiguous assemblies. Libraries were prepared using the Oxford Nanopore technologies (ONT) Native Barcoding Ligation kit (EXP-NBD114) according to manufacturer’s protocol, and sequenced on a PromethION 2 Solo platform with FLO-PRO114M flowcell to a target depth of 5 Gb per sample.
Metric
Metric
No cleanup
(control)
No cleanup
(control)
CamSelect
Long™
CamSelect
Long™
Improvement
(%)
Improvement
(%)
Metric
No cleanup
(control)
CamSelect
Long™
Improvement
(%)
Metric
No cleanup
(control)
CamSelect
Long™
Improvement
(%)
Total yield
1.7 Gb
5.5 Gb
223.50%
Total yield
1.7 Gb
5.5 Gb
223.50%
Read length N50
4,745 bp
7419 bp
56.40%
Read length N50
4,745 bp
7419 bp
56.40%
Mean read length
3416 bp
5152 bp
50.80%
Mean read length
3416 bp
5152 bp
50.80%
Long read fraction>10kb
4.70%
11.90%
153.20%
Long read fraction>10kb
4.70%
11.90%
153.20%
Stool-derived and saliva-derived DNA was analyzed on the Agilent TapeStation System before and after treatment with CamSelect LongTM. The results are depicted below.
Stool-derived and saliva-derived DNA was analyzed on the Agilent TapeStation System before and after treatment with CamSelect LongTM. The results are depicted below.
Post analysis
Post analysis
Untreated
sample
Untreated
sample
Sample treated with
Camselect Long™
Sample treated with
Camselect Long™
Post analysis
Untreated
sample
Sample treated with
Camselect Long™
Post analysis
Untreated
sample
Sample treated with
Camselect Long™
% reads mapping to human host
1.17
0.278
% reads mapping to human host
1.17
0.278
Assembled data
79 mb
192 mb
Assembled data
79 mb
192 mb
MAGS
43
116
MAGS
43
116
In stool samples, cleanup and size-selection prior to library preparation reduced host-mapped reads, increased total assembled sequence length, and substantially improved recovery of metagenome-assembled genomes (MAGs).
In stool samples, cleanup and size-selection prior to library preparation reduced host-mapped reads, increased total assembled sequence length, and substantially improved recovery of metagenome-assembled genomes (MAGs).
Purpose-built for long-read sequencing economics
Long-read whole-genome sequencing (WGS)
Metagenomics and microbiome sequencing
Structural variant detection
De novo genome assembly
MAG recovery and assembly
Purpose-built for long-read sequencing economics
Long-read whole-genome sequencing (WGS)
Metagenomics and microbiome sequencing
Structural variant detection
De novo genome assembly
MAG recovery and assembly
Purpose-built for long-read sequencing economics
Long-read whole-genome sequencing (WGS)
Metagenomics and microbiome sequencing
Structural variant detection
De novo genome assembly
MAG recovery and assembly
Purpose-built for long-read sequencing economics
Long-read whole-genome sequencing (WGS)
Metagenomics and microbiome sequencing
Structural variant detection
De novo genome assembly
MAG recovery and assembly
Workflow overview
Workflow overview
Workflow overview
Workflow overview
Workflow overview
Illumina NGS Library Prep
Illumina NGS Library Prep
Illumina NGS Library Prep
Illumina NGS Library Prep
NovaSeq
NovaSeq
NovaSeq
NovaSeq
NovaSeq
NextSeq
NextSeq
NextSeq
NextSeq
NextSeq
MiSeq
MiSeq
MiSeq
MiSeq
MiSeq
CamSelect NGS removes excess primers and unwanted fragments after PCR, ensuring cleaner libraries. In dual-index workflows, it’s also used post-indexing PCR to improve purity before sequencing.
Streamline your nucleic acid extraction with a magnetic stand that’s designed for consistency, speed, and ease of use.
Streamline your nucleic acid extraction with a magnetic stand that’s designed for consistency, speed, and ease of use.
CamSelect NGS removes excess primers and unwanted fragments after PCR, ensuring cleaner libraries. In dual-index workflows, it’s also used post-indexing PCR to improve purity before sequencing.
DNA extraction
DNA extraction
DNA extraction
DNA extraction
DNA extraction
PCR Amplification
PCR amplification
PCR amplification
Clean-up
Clean-up
Clean-up
PCR amplification
Clean-up
PCR amplification
Clean-up
Library QC
Library QC
Library QC
Library QC
Library QC
Normalization & pooling
Normalization & pooling
Normalization & pooling
Normalization & pooling
Normalization & pooling
Sequencing
Sequencing
Sequencing
Sequencing
Sequencing
Target Enrichment
Target Enrichment
Target Enrichment
Target Enrichment
Agilent SureSelect
Agilent SureSelect
Agilent SureSelect
Agilent SureSelect
Agilent SureSelect
IDT xGen
IDT xGen
IDT xGen
IDT xGen
IDT xGen
Twist
Twist
Twist
Twist
Twist
CamSelect NGS clean-up removes oligo contamination, excess primers, and short artifacts, delivering higher yield, greater purity, and more reliable sequencing in target enrichment workflows.
Streamline your nucleic acid extraction with a magnetic stand that’s designed for consistency, speed, and ease of use.
Streamline your nucleic acid extraction with a magnetic stand that’s designed for consistency, speed, and ease of use.
CamSelect NGS clean-up removes oligo contamination, excess primers, and short artifacts, delivering higher yield, greater purity, and more reliable sequencing in target enrichment workflows.
DNA extraction
DNA extraction
DNA extraction
DNA extraction
DNA extraction
Library preparation
Library preparation
Library preparation
Library preparation
Library preparation
Hybrid capture
Hybrid capture
Hybrid capture
Hybrid capture
Hybrid capture
NGS clean-up
NGS clean-up
NGS clean-up
NGS clean-up
NGS clean-up
QC and sequencing
QC and sequencing
QC and sequencing
QC and sequencing
QC and sequencing
Technical specifications
Technical specifications
Technical specifications
FAQs
FAQs
FAQs
Improve pore utilization
Elevate your sequencing workflows
Elevate your
sequencing workflows
Get more usable genomic data from every sequencing run.
Contact us now to learn how CamSelect NGS can improve your sequencing workflows.
Get more usable genomic data from every sequencing run.