Illumina DNA Prep with Exome 2.5 Enrichment v2, (S) Tagmentation Set B (96 Samples, 12-plex) 20155541 - Illumina

Illumina DNA Prep with Exome 2.5 Enrichment v2, (S) Tagmentation Set D (96 Samples, 12-plex)

Name: Illumina DNA Prep with Exome 2.5 Enrichment v2, (S) Tagmentation Set D (96 Samples, 12-plex)
Brand: Illumina
SKU: 20155543
Price: 8209.00 ILS
Availability: InStock

Vendor: Illumina

SKU: 20155543

8,209.00 NIS

Stock on Request

In stock

Includes Illumina DNA Prep with Enrichment library preparation and enrichment reagents, Twist Bioscience for Illumina Exome 2.5 Panel, Illumina Purification Beads, and Illumina DNA/RNA UD Indexes Set D, Tagmentation for whole exome enrichment of 96 libraries (eight, 12-plex enrichment reactions).

Illumina DNA Prep with Exome 2.5 Enrichment v2 kits offer a fast, high performing, and cost-effective workflow for reliable human whole-exome sequencing (WES).

Documents

Support Documentation

All Illumina DNA Prep with Exome 2.5 Enrichment v2 Support

Specifications

Area of interest Cancer research, Complex disease genomics, Consumer genomics, Genetic & rare diseases, Oncology, Population genomics, Reproductive health
Assay time 6.5 hr
Automation capability Liquid handling robot(s)
Content specifications Twist Bioscience for Illumina Exome 2.5 Exome 2.5 Panel 37.5 Mb coding content (≥ 99% of RefSeq, CCDS, ClinVar and ACMG pathogenic/likely pathogenic variants, COSMIC Cancer Gene Census), OMIM Twist Bioscience for Illumina Mitochondrial Panel covers the circular mitochondrial genome ChrM (16,659 bp, 37 genes)
Hands on time ~2 hr
Input quantity 50–1000 ng DNA
Instruments NextSeq 1000 SystemNextSeq 2000 SystemNextSeq 550 SystemNextSeq 550Dx in Research ModeNovaSeq 6000 SystemNovaSeq 6000Dx in Research ModeNovaSeq X Plus SystemNovaSeq X System
Key use Inherited disease variant analysis, Rare and undiagnosed disease variant analysis, Targeted analysis
Mechanism of action Bead-linked transposome and hybrid-capture chemistry
Method Exome sequencing, Target enrichment, Targeted DNA sequencing
Multiplexing Pre-enrichment pooling of up to 12-plex is tested. Kit configuration supports multiplexing up to 192 samples, up to 384 samples is possible with added unique dual index sets.
Nucleic acid type DNA
Specialized sample types Blood, Saliva
Species category Human
Sub category Library preparation kits
Technology Sequencing
Variant class Copy number variants (CNVs), Germline variants, Insertions-deletions (indels), Loss of heterozygosity (LOH), Single nucleotide polymorphisms (SNPs), Single nucleotide variants (SNVs)

links and documants

Datasheet url Click here
Source url Click here