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White Papers

Podcast 1 - NGS & Autism Transcript

22 Oct 2013

Application Notes

High Throughput TruSeq Stranded mRNA Library Construction on the Biomek FXP

22 Oct 2013

Application Notes

Automated TruSeq DNA Sample Preparation using Biomek FXP Liquid Handler

22 Oct 2013

Application Notes

Automated TruSeq RNA Sample Preparation from FFPE Tissue Specimens utilizing the Biomek FXP Liquid Handler

21 Oct 2013

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

Highly Efficient MicroRNA and Total RNA Purification from Formalin-Fixed Paraffin-Embedded Tissues (FFPE)

12 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

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

20 Aug 2013

Application Notes

Development and Validation of Automated Methods for Next-Generation Sequencing Library Preparation & Exome Capture

8 Aug 2013

Application Notes

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

28 Jul 2013

Scientific Posters

Detection of Copy Number and Loss of Heterozygosity with OGTS’s ISCA

16 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

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

Scientific Posters

Accurate IGN Cancer Sequencing with a Combined-Calling Method

8 Jul 2013

Case Studies

Recent Discoveries in Cancer Genomics

2 Jul 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

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Podcast 1 - NGS & Autism Transcript

High Throughput TruSeq Stranded mRNA Library Construction on the Biomek FX<sup>P</sup>

Automated TruSeq DNA Sample Preparation using Biomek FX<sup>P</sup> Liquid Handler

Automated TruSeq RNA Sample Preparation from FFPE Tissue Specimens utilizing the Biomek FX<sup>P</sup> Liquid Handler

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

Highly Efficient MicroRNA and Total RNA Purification from Formalin-Fixed Paraffin-Embedded Tissues (FFPE)

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

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

Development and Validation of Automated Methods for Next-Generation Sequencing Library Preparation & Exome Capture

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

Detection of Copy Number and Loss of Heterozygosity with OGTS’s ISCA

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

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

Accurate IGN Cancer Sequencing with a Combined-Calling Method

Recent Discoveries in Cancer Genomics

Accurate IGN Cancer Sequencing with a Combined-Calling Method

Deep Exome Sequencing Helps Researchers to Discover Causative Mutations

Resources

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Selected Filters:

Podcast 1 - NGS & Autism Transcript

High Throughput TruSeq Stranded mRNA Library Construction on the Biomek FX<sup>P</sup>

Automated TruSeq DNA Sample Preparation using Biomek FX<sup>P</sup> Liquid Handler

Automated TruSeq RNA Sample Preparation from FFPE Tissue Specimens utilizing the Biomek FX<sup>P</sup> Liquid Handler

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

Highly Efficient MicroRNA and Total RNA Purification from Formalin-Fixed Paraffin-Embedded Tissues (FFPE)

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

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

Development and Validation of Automated Methods for Next-Generation Sequencing Library Preparation & Exome Capture

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

Detection of Copy Number and Loss of Heterozygosity with OGTS’s ISCA

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

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

Accurate IGN Cancer Sequencing with a Combined-Calling Method

Recent Discoveries in Cancer Genomics

Accurate IGN Cancer Sequencing with a Combined-Calling Method

Deep Exome Sequencing Helps Researchers to Discover Causative Mutations

Resources Filter