Strand Life Sciences announces the release of Strand NGS v3.1 at ASHG 2017
...theme is large-scale RNA-Seq data analysis. Current cross-cohort RNA...includes confounding variable analysis to eliminate technical ef...ccuracy and efficiency of NGS data analysis. Customers can look forward t...gnostics and clinical genomic data interpretation using a strong fou...2443 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.2681 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...2681 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...2674 days ago
SeqMule: Automated human exome/genome variants detection
SeqMule takes single-end or paird-end FASTQ or BAM files, gen...ript consisting of more than 10 popular alignment, analysis tools and runs the script...ersection among different callers, and downloading databases. SeqMule can be used for bot...2673 days ago
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Pacbio Long Reads Compatible Software and Tools
The following software packages are known...be compatible with PacBio® data, in addition to PacBio's own SMRT® Analysis suite. All packages are b...open source software for PacBio data? Email us. Software categor...sensus and variant calling RNA analysis Epigenetic base modification...2665 days ago
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