Package: idemuxcpp
Version: 0.3.0-1
Architecture: amd64
Maintainer: Lexogen <gregor.entzian@lexogen.com>
Installed-Size: 27105
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: 2389460
MD5sum: b339c3c052dfc7752888e26763a91a4c
SHA1: 88725f325efd72bb4d7058b9a4e6d7f0692dc49e
SHA256: bb65ecf1ad3139eaeebde88b2721baca53702f0438672a9fdb4b308bb4e2d9cb
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.