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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

Scientific Posters

Gel-Free Size Selection Using SPRIselect For Next Generation Sequencing

25 Jun 2013

Application Notes

Estimating Sequencing Coverage

24 Jun 2013

Application Notes

Whole Genome Trio Analysis

20 Jun 2013

Application Notes

Tumor Heterogeneity Findings Impact Personalized Medicine Approaches

18 Jun 2013

Application Notes

Considerations for Next-Gen Sequence Assembly and Analysis Software Selection

16 Jun 2013

Application Notes

Multiplex Sequence Capture for Targeted Resequencing of Candidate Gene Panels in Cancer

27 May 2013

Application Notes

Amplicon Analysis of Lung Cancer Samples

23 May 2013

Application Notes

Solving the Cancer Puzzle with Next Generation Sequencing and Microarrays

20 May 2013

Application Notes

Next-Generation Amplicon-Based Deep Sequencing and Its Application to Characterize Hematological Malignancies

16 May 2013

Application Notes

Automation of Illumina TruSeq Exome Enrichment Using the Agilent Bravo Liquid Handling Platform

15 May 2013

Application Notes

Amplicon Sequencing from FFPE Tissues on the MiSeq® System

8 May 2013

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Selected Filters:

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

Gel-Free Size Selection Using SPRIselect For Next Generation Sequencing

Estimating Sequencing Coverage

Whole Genome Trio Analysis

Tumor Heterogeneity Findings Impact Personalized Medicine Approaches

Considerations for Next-Gen Sequence Assembly and Analysis Software Selection

Multiplex Sequence Capture for Targeted Resequencing of Candidate Gene Panels in Cancer

Amplicon Analysis of Lung Cancer Samples

Solving the Cancer Puzzle with Next Generation Sequencing and Microarrays

Next-Generation Amplicon-Based Deep Sequencing and Its Application to Characterize Hematological Malignancies

Automation of Illumina TruSeq Exome Enrichment Using the Agilent Bravo Liquid Handling Platform

Amplicon Sequencing from FFPE Tissues on the MiSeq® System

Resources

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Search

Selected Filters:

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

Gel-Free Size Selection Using SPRIselect For Next Generation Sequencing

Estimating Sequencing Coverage

Whole Genome Trio Analysis

Tumor Heterogeneity Findings Impact Personalized Medicine Approaches

Considerations for Next-Gen Sequence Assembly and Analysis Software Selection

Multiplex Sequence Capture for Targeted Resequencing of Candidate Gene Panels in Cancer

Amplicon Analysis of Lung Cancer Samples

Solving the Cancer Puzzle with Next Generation Sequencing and Microarrays

Next-Generation Amplicon-Based Deep Sequencing and Its Application to Characterize Hematological Malignancies

Automation of Illumina TruSeq Exome Enrichment Using the Agilent Bravo Liquid Handling Platform

Amplicon Sequencing from FFPE Tissues on the MiSeq® System

Resources Filter