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Strand Life Sciences announces the release of Strand NGS v3.1 at ASHG 2017
...ace allows the specification of custom UMI protocols. “For liquid biopsies and low-grade FFPE samples, UMI support in DNA-Seq enables the detection of somatic variants at low co...2371 days ago
SeqMule: Automated human exome/genome variants detection
SeqMule takes single-end or paird-end FASTQ or BAM files, generates a script consisting of more than 10 popular alignment, analysis tools and runs the script line by lin...2601 days ago
Pacbio Long Reads Compatible Software and Tools
...ftware. Know of any other open source software for PacBio data? Email us. Software categories: De novo assembly Structural Variations Detection Reference-based alignment C...2593 days ago
LoRDEC: a hybrid error correction program for long, PacBio reads
...ss substitutions. LoRDEC can correct errors of all these types. After correction, a larger portion of the sequence of PacBio reads is usable for detection of region of similarity with...2567 days ago
DeCoSTAR - Detection of Co-evolution
DeCoSTAR is a software which aims at reconstructing ancestral gene or genome organizations, in the form of sets of neighborhood relations -adjacencies- between pairs of...2563 days ago
npScarf: Scaffolding and Completing Assemblies in Real-time Fashion
...on a laptop computer for microbial datasets. It also facilitates the real-time analysis of positional information such as gene ordering and the detection of genes from mobile elements...2524 days ago