Results for "Rare variants"
News
A team from Cold Spring Harbor Laboratory has released an algorithm, called Scalpel...heir unaffected siblings, a pattern that persisted even after excluding common variants.3536 days ago
- Dr Eric Londin, Assistant Professor, Thomas Jefferson U...ng more than 40 percent of disease-causing genetic variants, and we found that the worst-...forming method missed more than 90 percent of such variants in four of the 56 genes," he...
3615 days ago
- In less than two weeks, NCBI will offer a webinar entitled "Introducing 3 NCBI Resources to Navigate Testing for Disease Linked Variants: MedGen, GTR and ClinVar". Th...
3609 days ago
Webinar on Streamlining large scale analysis using the Strand NGS Pipeline Manager on 24 Feb 2016
Live Webinar on Streamlining large scale NGS data analysis using the Strand NGS Pip...gns reads, filters poor-quality matches, computes coverage metrics, identifies variants, checks for sample cross-cont...3002 days ago
- A recent Nature Biotechnology paper from Chunyu Han’s lab, DNA-guided genome editing using the&nb...vage in our experiments. Second, 5′ phosphorylated short ssDNAs are rare in...
2900 days ago
Webinar on Fast and Accurate DNA Variant Calling on 26 Apr 2017
Continuing our DNA-Seq webinar series, we'll present Strand NGS v3.0 best-practices: a workflow that identifies highly accurate variants from raw reads. Our best prac...2561 days ago
Strand Life Sciences announces the release of Strand NGS v3.1 at ASHG 2017
Strand Life Sciences announces the release of Strand NGS v3.1 at ASHG 2017 ORLANDO...ow-grade FFPE samples, UMI support in DNA-Seq enables the detection of somatic variants at low concentrations. In RNA...2376 days ago
- ...-tagged NGS libraries allow, ultra-sensitive detection of low frequency variants from liquid biopsy sample...ly analyse UMI-tagged NGS data helping researchers and labs involved in rare variant calling like in cfDNA bas...
2361 days ago
- Live webinar on Analysis of Variants using GeneSpring GX 14.9 on 6th Dec at 8 AM PSTVariant analysis workfl...pring GX is designed for detection, management and analysis of genetic variants such as single nucleotide pol...
2353 days ago
- ...andard analysis tools to detect wide range of variants. Strand Life Sciences, ha...ples using multi-gene panels for diagnosis of rare disease conditions. NGS data anal...software can easily detect single nucleotide variants, the complex ones involving i...
2299 days ago
