Resources

Results per page

Selected Filters:

Oxford Gene Technology Ltd Clear Filters

Application Notes

SureSeq: Variant calling best practices

26 Sept 2023

Application Notes

Ordering information and troubleshooting tips for NGS

4 Jul 2023

Scientific Posters

Development of a target-capture NGS assay for use in molecular-based research of myeloid measurable residual disease

4 Jul 2023

Application Notes

Six tips to improve sequencing libraries

4 Jul 2023

Application Notes

Evaluation of Enzymatic DNA Digestion as an Alternative to Mechanical DNA Fragmentation (Sonication) for Targeted NGS using the SureSeq™ Myeloid Panel

22 Aug 2016

Application Notes

Evaluation of DNA Labeling Kits for Enhanced Microarray Results

22 Apr 2014

Application Notes

Comprehensive Genomic Analysis – Complementing Sequencing with High-Resolution CNV Detection

9 Apr 2014

White Papers

Comprehensive Genomic Analysis – Complementing Sequencing with High-Resolution CNV Detection

26 Feb 2014

White Papers

The Importance of Enrichment Assay Choice and Optimization for Confident Variant Detection

29 Nov 2013

Scientific Posters

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

16 Jul 2013

White Papers

When to Use Targeted Resequencing — Choosing the Right NGS Method

16 Jul 2013

Application Notes

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

27 Jun 2013

Application Notes

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

26 Mar 2013

Application Notes

Comprehensive Data Analysis for Targeted Next Generation Sequencing

4 Sept 2012

Application Notes

Focusing On Results Not Data — Comprehensive Data Analysis for Targeted Next Generation Sequencing

1 Aug 2012

Application Notes

Fishing for Variants in the Deep End of the Gene Pool: OGT’s Custom Bait Designs

24 May 2012

Resources

Resources Filter

Search

Selected Filters:

SureSeq: Variant calling best practices

Ordering information and troubleshooting tips for NGS

Development of a target-capture NGS assay for use in molecular-based research of myeloid measurable residual disease

Six tips to improve sequencing libraries

Evaluation of Enzymatic DNA Digestion as an Alternative to Mechanical DNA Fragmentation (Sonication) for Targeted NGS using the SureSeq™ Myeloid Panel

Evaluation of DNA Labeling Kits for Enhanced Microarray Results

Comprehensive Genomic Analysis – Complementing Sequencing with High-Resolution CNV Detection

Comprehensive Genomic Analysis – Complementing Sequencing with High-Resolution CNV Detection

The Importance of Enrichment Assay Choice and Optimization for Confident Variant Detection

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

When to Use Targeted Resequencing — Choosing the Right NGS Method

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

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

Comprehensive Data Analysis for Targeted Next Generation Sequencing

Focusing On Results Not Data — Comprehensive Data Analysis for Targeted Next Generation Sequencing

Fishing for Variants in the Deep End of the Gene Pool: OGT’s Custom Bait Designs

Resources

Resources FilterResources Filter

Search

Selected Filters:

SureSeq: Variant calling best practices

Ordering information and troubleshooting tips for NGS

Development of a target-capture NGS assay for use in molecular-based research of myeloid measurable residual disease

Six tips to improve sequencing libraries

Evaluation of Enzymatic DNA Digestion as an Alternative to Mechanical DNA Fragmentation (Sonication) for Targeted NGS using the SureSeq™ Myeloid Panel

Evaluation of DNA Labeling Kits for Enhanced Microarray Results

Comprehensive Genomic Analysis – Complementing Sequencing with High-Resolution CNV Detection

Comprehensive Genomic Analysis – Complementing Sequencing with High-Resolution CNV Detection

The Importance of Enrichment Assay Choice and Optimization for Confident Variant Detection

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

When to Use Targeted Resequencing — Choosing the Right NGS Method

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

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

Comprehensive Data Analysis for Targeted Next Generation Sequencing

Focusing On Results Not Data — Comprehensive Data Analysis for Targeted Next Generation Sequencing

Fishing for Variants in the Deep End of the Gene Pool: OGT’s Custom Bait Designs

Resources Filter