Package: idemuxcpp
Version: 0.3.0-1
Architecture: amd64
Maintainer: Lexogen <gregor.entzian@lexogen.com>
Installed-Size: 27109
Depends: libboost-filesystem1.74.0 (>= 1.74.0), libboost-iostreams1.74.0 (>= 1.74.0), libc6 (>= 2.34), libgcc-s1 (>= 3.3.1), libstdc++6 (>= 11), zlib1g (>= 1:1.2.2), zlib1g-dev (>= 1.2.8), libboost-dev (>= 1.55), libboost-filesystem-dev (>= 1.55), libboost-system-dev (>= 1.55), libboost-iostreams-dev (>= 1.55), libbamtools-dev (>= 2.3.0)
Conflicts: idemuxcpp
Provides: idemuxcpp
Filename: amd64/idemuxcpp_0.3.0-1_amd64.deb
Size: 2390128
MD5sum: b4dcf97ba7f41e4683d6273cff425e32
SHA1: 202998533bb980c1a487974d6a44c9a498709662
SHA256: c68fcb0502752c7c0cb05ddbaac71315803625c0e8d2e2560dfbc8d0e004bfc4
Section: science
Priority: optional
Description: Demultiplex RNA-seq reads from fastq.gz files into separate files according to their indices.
 Idemux can demultiplex based on i7, i5, and i1 inline barcodes. While this tool
 can generally be used to demultiplex any barcodes (as long as they are
 correctly supplied and in the fastq header), it performs best when used in
 combination with Lexogen indices, as it will correct common sequencing errors
 in the sequenced barcodes. This will allow you to retain more reads from your
 sequencing experiment while minimizing cross contamination.