Package: idemuxcpp
Version: 0.3.0-1
Architecture: amd64
Maintainer: Lexogen <gregor.entzian@lexogen.com>
Installed-Size: 27177
Depends: libboost-filesystem1.65.1, libboost-iostreams1.65.1, libboost-system1.65.1, libc6 (>= 2.14), libgcc1 (>= 1:3.0), libstdc++6 (>= 7), 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: 2224956
MD5sum: 23c192f78c6ca1e141a0bb0b5021d7fc
SHA1: 8319479d322f563d5095865c0de72da0dae674f4
SHA256: 433f46b0204f8372a1dd0acb8a22d7f1ea7ce8bfae29eeb84e660dff70d7d08c
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.