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Application Note

SureSeq: Variant calling best practices

26 Sept 2023

Application Note

Ordering information and troubleshooting tips for NGS

4 Jul 2023

Scientific Poster

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

4 Jul 2023

Application Note

Six tips to improve sequencing libraries

4 Jul 2023

Application Note

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 Note

Evaluation of DNA Labeling Kits for Enhanced Microarray Results

22 Apr 2014

Application Note

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 Poster

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 Note

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

27 Jun 2013

Application Note

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

26 Mar 2013

Application Note

Comprehensive Data Analysis for Targeted Next Generation Sequencing

4 Sept 2012

Application Note

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

1 Aug 2012

Application Note

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

24 May 2012

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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

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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