13
edits
Changes
Update of all fields.
{{Bioinformatics application
|sw summary=de novo and reference assembly of Sanger, 454, Solexa, Helicos, and SOLiD data. Commercial next-gen-seq software that extends the CLCbio Main Workbench software. Includes SNP detection, browser and other features. Runs on Windows, Mac OS X and Linux.
|bio domain=Genomics, Whole Genome Resequencing, De-novo assembly, SNP discovery, InDel discovery, ChIP-Seq, InDel discovery, RNA-Seq,|bio method=Mapping, Assembly, Alignments, command line tool wrappers, genetic variation annotation, Statistics, Visualisation,|bio tech=454, Solexa, Solid, Helicos, Sanger, |created by=Thomas Knudsen and Bjarne Knudsen et al|created at=CLC bio|maintained=Yes|input format=FASTA, FASTQ, A reference genome sequence in fasta format, GenBank, SAM, Illumina Bustard, ELAND, CSFASTA/CSQUAL (ABI SOLiD), and many more.|output format=FASTA, FASTQ, GFF, GenBank, Nexus, and more|sw feature=Advanced and user-friendly analyses of genomic, transcriptomic and epigenomic NGS data in a graphical user-interface|language=Java and C++|licence=Perpetual and temporal|os=Windows, Mac OS X, Linux,
}}
Link: http://www.clcbio.com/index.php?id=1240 Category: Integrated solutions
