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...): “The useful features of NgAgo for genome editing include the following.First, it has a low tolerance to guide–target mismatch. A single nucleotide mismatch at each p...2965 days ago
Strand Life Sciences announces the release of Strand NGS v3.1 at ASHG 2017
...es, UMI support in DNA-Seq enables the detection of somatic variants at low concentrations. In RNA-Seq, large-scale and UMI support can be used in single-cell-based studies that revea...2441 days ago
- ....9 on 6th Dec at 8 AM PSTVariant analysis workflow in GeneSpring GX is designed for detection, management and analysis of genetic variants such as single nucleotide polymorphisms (SNP...
2418 days ago
- ...nd cost of testing. Testing involves massively parallel sequencing of a single to 100s of genes in a one ass...ting using StrandOMICS. While most analysis software can easily detect single nucleotide variants, the comp...
2364 days ago
- ...perform a comprehensive genetic testing in a cost-effective manner. Thus, with the advent of NGS technology, the possibility of offering a ‘single platform solution’ for...
2294 days ago
Phased Human Genome Assembly !
...nbsp;de novo scaffolded using Phase Genomics’ Proximo Hi-C platform, resulting in the first chromosome-scale diploid assembly of a single individual accomplished with...2091 days ago
NGS Platforms launched by BGI’s MGI Tech
...s for $1 million. The T7 enables simultaneous but independent operation of up to four flow cells, which means different applications such as single-cell RNA sequencing, whole ex...1997 days ago
Complete genome sequence of Wuhan seafood market pneumonia virus is out !
...Several are identical and none has more than 5 differences (99.983% similarity). This strongly suggests that transmission into humans came from a single pointed source and happened v...1611 days ago
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