Package: idemuxcpp
Version: 0.1.7-1
Architecture: amd64
Maintainer: Lexogen <gregor.entzian@lexogen.com>
Installed-Size: 12249
Depends: libboost-filesystem1.67.0, libboost-iostreams1.67.0, libboost-system1.67.0, libc6 (>= 2.14), libgcc1 (>= 1:3.0), libgomp1 (>= 4.9), libstdc++6 (>= 6), zlib1g (>= 1:1.1.4), zlib1g-dev (>= 1.2.8), libboost-dev (>= 1.55), libboost-filesystem-dev (>= 1.55), libboost-system-dev (>= 1.55), libboost-iostreams-dev (>= 1.55)
Conflicts: idemuxcpp
Provides: idemuxcpp
Filename: ./amd64/idemuxcpp_0.1.7-1_amd64.deb
Size: 1211576
MD5sum: 0485c0861b023412af6ebb2ff01dcca3
SHA1: 3536d0b9c28eb3922a07559f7b949ca2788bb6c4
SHA256: cbacce4d8703ab5a145da03f70f9e0a169c614cf77d54661cabc2f9e7dcb7f98
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.