Package: idemuxcpp
Version: 0.2.0-1
Architecture: amd64
Maintainer: Lexogen <gregor.entzian@lexogen.com>
Installed-Size: 27197
Depends: libboost-filesystem1.71.0, libboost-iostreams1.71.0, libc6 (>= 2.14), libgcc-s1 (>= 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), libbamtools-dev (>= 2.3.0)
Conflicts: idemuxcpp
Provides: idemuxcpp
Filename: amd64/idemuxcpp_0.2.0-1_amd64.deb
Size: 2225332
MD5sum: da0fd9de0ff5f1e2439878b7b1fac4f6
SHA1: f9dfb346cc270f3ee8abcfa301521540b890751b
SHA256: 2a6149c2ebbfbecc338c31d01b9d11cce49f741e1c22ca019d1656e7165bbdf9
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.