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DNA Sequencing Clear Filters

White Papers

Clinical Next Generation Sequencing, the Dawn of a New Era

21 Oct 2013

Case Studies

Tag Team: Scientists Use Pippin to Optimize Nextera Libraries

16 Sept 2013

Case Studies

New Take on RADseq Enables High-Throughput Variant Discovery

16 Sept 2013

Case Studies

Better Metagenomics Methods Offer Hope for Studies with Ultra-Low DNA

15 Sept 2013

Application Notes

ChIP-Seq Library Prep Using the Pippin Prep DNA Size Selection System

10 Sept 2013

Scientific Posters

Gene, Transcription Start Site and Splice Site Identification Increased Through Use of Automated Preparative Gel Electrophoresis

9 Sept 2013

Application Notes

Cambridge Epigenetix TrueMethyl™ Beta Trial

3 Sept 2013

Application Notes

Agrigenomics Genotyping Decisions Reach Crossroads

1 Sept 2013

Application Notes

Nextera Sample Preparation for the MiSeq System

22 Aug 2013

Application Notes

Evaluation of the PowerPlex® Fusion System for Use on the ABI PRISM® 310 Genetic Analyzer

19 Aug 2013

Application Notes

Screening Cancer Genes Using NimbleGen Sequence Capture Arrays and the GS Junior Sequencing System

28 Jul 2013

Application Notes

SSCP analysis in exon 6 of the tumor suppressor gene p53

25 Jul 2013

Application Notes

From Minuscule Amounts to Magnificent Results: Reliable ChIP-seq Data from 10,000 cells with True MicroChIP™ and MicroPlex Library Preparation™ Kits

16 Jul 2013

Application Notes

Molecular Beacon Based Helicase Assays Using a Microplate Reader

16 Jul 2013

White Papers

When to Use Targeted Resequencing — Choosing the Right NGS Method

16 Jul 2013

Application Notes

High Resolution LabChip XT Fractionation of Illumina Compatible Small RNA Libraries using the DNA 300 Assay Kit

9 Jul 2013

Application Notes

Detecting Copy Number Variants and Runs of Homozygosity on a Single Array — Challenges and Applications

27 Jun 2013

Application Notes

Rapid and Reliable Methylation Detection in Archival Tissue Samples using High-Resolution Melting Analysis

27 Jun 2013

Scientific Posters

Accurate IGN Cancer Sequencing with a Combined-Calling Method

27 Jun 2013

Application Notes

Deep Exome Sequencing Helps Researchers to Discover Causative Mutations

26 Jun 2013

Application Notes

Copy-neutral Loss of Heterozygosity in Cancer

24 Jun 2013

Application Notes

Estimating Sequencing Coverage

24 Jun 2013

Scientific Posters

Cancer and Metastasis Signaling Pathways

23 Jun 2013

Application Notes

Whole Genome Trio Analysis

20 Jun 2013

Application Notes

SSCP Analysis on GenePhor: A Screening Method for BRCA1 Point Mutations

18 Jun 2013

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Selected Filters:

Clinical Next Generation Sequencing, the Dawn of a New Era

Tag Team: Scientists Use Pippin to Optimize Nextera Libraries

New Take on RADseq Enables High-Throughput Variant Discovery

Better Metagenomics Methods Offer Hope for Studies with Ultra-Low DNA

ChIP-Seq Library Prep Using the Pippin Prep DNA Size Selection System

Gene, Transcription Start Site and Splice Site Identification Increased Through Use of Automated Preparative Gel Electrophoresis

Cambridge Epigenetix TrueMethyl™ Beta Trial

Agrigenomics Genotyping Decisions Reach Crossroads

Nextera Sample Preparation for the MiSeq System

Evaluation of the PowerPlex® Fusion System for Use on the ABI PRISM® 310 Genetic Analyzer

Screening Cancer Genes Using NimbleGen Sequence Capture Arrays and the GS Junior Sequencing System

SSCP analysis in exon 6 of the tumor suppressor gene p53

From Minuscule Amounts to Magnificent Results: Reliable ChIP-seq Data from 10,000 cells with True MicroChIP™ and MicroPlex Library Preparation™ Kits

Molecular Beacon Based Helicase Assays Using a Microplate Reader

When to Use Targeted Resequencing — Choosing the Right NGS Method

High Resolution LabChip XT Fractionation of Illumina Compatible Small RNA Libraries using the DNA 300 Assay Kit

Detecting Copy Number Variants and Runs of Homozygosity on a Single Array — Challenges and Applications

Rapid and Reliable Methylation Detection in Archival Tissue Samples using High-Resolution Melting Analysis

Accurate IGN Cancer Sequencing with a Combined-Calling Method

Deep Exome Sequencing Helps Researchers to Discover Causative Mutations

Copy-neutral Loss of Heterozygosity in Cancer

Estimating Sequencing Coverage

Cancer and Metastasis Signaling Pathways

Whole Genome Trio Analysis

SSCP Analysis on GenePhor: A Screening Method for BRCA1 Point Mutations

Resources

Resources FilterResources Filter

Search

Selected Filters:

Clinical Next Generation Sequencing, the Dawn of a New Era

Tag Team: Scientists Use Pippin to Optimize Nextera Libraries

New Take on RADseq Enables High-Throughput Variant Discovery

Better Metagenomics Methods Offer Hope for Studies with Ultra-Low DNA

ChIP-Seq Library Prep Using the Pippin Prep DNA Size Selection System

Gene, Transcription Start Site and Splice Site Identification Increased Through Use of Automated Preparative Gel Electrophoresis

Cambridge Epigenetix TrueMethyl™ Beta Trial

Agrigenomics Genotyping Decisions Reach Crossroads

Nextera Sample Preparation for the MiSeq System

Evaluation of the PowerPlex® Fusion System for Use on the ABI PRISM® 310 Genetic Analyzer

Screening Cancer Genes Using NimbleGen Sequence Capture Arrays and the GS Junior Sequencing System

SSCP analysis in exon 6 of the tumor suppressor gene p53

From Minuscule Amounts to Magnificent Results: Reliable ChIP-seq Data from 10,000 cells with True MicroChIP™ and MicroPlex Library Preparation™ Kits

Molecular Beacon Based Helicase Assays Using a Microplate Reader

When to Use Targeted Resequencing — Choosing the Right NGS Method

High Resolution LabChip XT Fractionation of Illumina Compatible Small RNA Libraries using the DNA 300 Assay Kit

Detecting Copy Number Variants and Runs of Homozygosity on a Single Array — Challenges and Applications

Rapid and Reliable Methylation Detection in Archival Tissue Samples using High-Resolution Melting Analysis

Accurate IGN Cancer Sequencing with a Combined-Calling Method

Deep Exome Sequencing Helps Researchers to Discover Causative Mutations

Copy-neutral Loss of Heterozygosity in Cancer

Estimating Sequencing Coverage

Cancer and Metastasis Signaling Pathways

Whole Genome Trio Analysis

SSCP Analysis on GenePhor: A Screening Method for BRCA1 Point Mutations

Resources Filter