bionic (1) cuffcompare.1.gz

Provided by: cufflinks_2.2.1+dfsg.1-2_amd64 bug

NAME

       cuffcompare - component of cufflinks suite

DESCRIPTION

       cuffcompare  v2.2.1  ()  -----------------------------  Usage: cuffcompare [-r <reference_mrna.gtf>] [-R]
       [-T] [-V] [-s <seq_path>]

              [-o  <outprefix>]  [-p  <cprefix>]  {-i   <input_gtf_list>   |   <input1.gtf>   [<input2.gtf>   ..
              <inputN.gtf>]}

              Cuffcompare  provides  classification,  reference  annotation  mapping  and various statistics for
              Cufflinks transfrags.  Cuffcompare clusters and tracks transfrags across multiple samples, writing
              matching    transcripts    (intron   chains)   into   <outprefix>.tracking,   and   a   GTF   file
              <outprefix>.combined.gtf containing a nonredundant set of transcripts across all input files (with
              a single representative transfrag chosen for each clique of matching transfrags across samples).

OPTIONS

       -i provide a text file with a list of Cufflinks GTF files to process instead

              of  expecting  them  as  command line arguments (useful when a large number of GTF files should be
              processed)

       -r a set of known mRNAs to use as a reference for assessing

              the accuracy of mRNAs or gene models given in <input.gtf>

       -R for -r option, consider only the reference transcripts that

              overlap any of the input transfrags (Sn correction)

       -Q for -r option, consider only the input transcripts that

              overlap any of the reference transcripts (Sp correction); (Warning: this will discard all  "novel"
              loci!)

       -M  discard  (ignore)  single-exon  transfrags  and reference transcripts -N discard (ignore) single-exon
       reference transcripts

       -s <seq_path> can be a multi-fasta file with all the genomic sequences or

              a directory containing multiple single-fasta files (one file per contig); lower case bases will be
              used to classify input transcripts as repeats

       -e max. distance (range) allowed from free ends of terminal exons of reference

              transcripts when assessing exon accuracy (100)

       -d  max.  distance  (range)  for  grouping  transcript  start  sites  (100) -p the name prefix to use for
       consensus transcripts in the

              <outprefix>.combined.gtf file (default: 'TCONS')

       -C include the "contained" transcripts in the .combined.gtf  file  -F  do  not  discard  intron-redundant
       transfrags if they share the 5' end

              (if they differ only at the 3' end))

       -G generic GFF input file(s): do not assume Cufflinks GTF, do not

              discard any intron-redundant transfrags)

       -T  do  not  generate .tmap and .refmap files for each input file -V verbose processing mode (showing all
       GFF parsing warnings)