Results for "DISCOVAR"
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DISCOVAR is a new variant caller and DISCOVAR de novo a new genome assembler, both design...ntinuity that was not previously possible. DISCOVAR can call variants on a region...potentially tiling an entire large genome. DISCOVAR variant calling is under acti...2930 days ago
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Genome Assembly Tools and Software - PART2 !!
...NGS and assemblers into longer chromosomal fragments using comparative genome information and paired-end reads. DISCOVAR 51750 – Genome Shotgun Assembler and Variant CallerDISCOVAR is a whole genome shotgu...2677 days ago
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- DISCOVAR is a new variant caller and DISCOVAR de novo a new genome assembler, both designed for state-of-the-art data. Their inputs are chosen to optimize quality while keeping costs low. Currently it takes as input Illumina reads of length 250 or longer — produced on MiSeq or HiSeq 2500 &m...
Tags: Bioinformatics, NGS, Assembly, DISCOVAR, Variants, BroadInstitute
2930 days ago
