Strand Life Sciences announces the release of Strand NGS v3.1 at ASHG 2017
...rst theme is large-scale RNA-Seq data analysis. Current cross-cohort RNA....1 includes confounding variable analysis to eliminate technical ef...e accuracy and efficiency of NGS data analysis. Customers can look forward t...diagnostics and clinical genomic data interpretation using a strong fou...2437 days ago
FinisherSC: a repeat-aware and scalable tool for upgrading de novo assembly using long reads
FinisherSC, a repeat-aware and scalable tool for upgrading de novo assembly using long reads. Experiments with real data suggest that FinisherSC can provide longer and higher quality contigs than existing tools while maintaining high concordance.2675 days ago
PBSuite: Software for Long-Read Sequencing Data from PacBio
PBJelly - the genome upgrading tool. PBHoney - the structural variation discovery tool Both are contained within the PBSuite code found in downloads.----- PBJe...2675 days ago
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CONCOCT: Clustering cONtigs with COverage and ComposiTion
A program for unsupervised binning of metagenomic contigs by using nucleotide composition, coverage data in multiple samples and linkage data fro...2668 days ago
SeqMule: Automated human exome/genome variants detection
...files, generates a script consisting of more than 10 popular alignment, analysis tools and runs the script...n diagram showing intersection among different callers, and downloading databases. SeqMule can be used for bot...2667 days ago
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Pacbio Long Reads Compatible Software and Tools
...nown to be compatible with PacBio® data, in addition to PacBio's own SMRT® Analysis suite. All packages are b...other open source software for PacBio data? Email us. Software categor...nt Consensus and variant calling RNA analysis Epigenetic base modification...2658 days ago
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