3918 days ago
2885 days ago
Strand Life Sciences announces the release of Strand NGS v3.1 at ASHG 2017
...company. Founded in 2000, Strand is a leader in technology innovations for healthcare using genomics. By enhancing sequence-based diagnostics and clinical genomic data interpretation u...2397 days ago
Platypus: A Haplotype-Based Variant Caller For Next Generation Sequence Data
...ted capture data, it has been run on very large datasets as part of the Thousand Genomes and WGS500 projects, and is being used in clinical sequencing trials in the ...2030 days ago
1963 days ago
EXCAVATOR: detecting copy number variants from whole-exome sequencing data
...that EXCAVATOR outperforms the other methods and is therefore a valuable tool for the investigation of CNVs in largescale projects, as well as in clinical research and diagnostics. EXC...1959 days ago
Genome in a Bottle (GIAB) Consortium
...e technical infrastructure (reference standards, reference methods, and reference data) to enable translation of whole human genome sequencing to clinical practice. https://www.nist....1573 days ago
Dahak: benchmarking and containerization of tools for analysis of complex non-clinical metagenomes.
Dahak is a software suite that integrates state-of-the-art open source tools for metagenomic analyses. Tools in the dahak software suite will perform various steps in me...1498 days ago
1360 days ago
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