SHORE Subprograms
Contents
- 1 shore preprocess
- 2 shore import
- 3 shore mapflowcell
- 4 shore correct4pe
- 5 shore merge
- 6 shore mapview
- 7 shore consensus
- 8 shore qVar
- 9 shore methyl
- 10 shore coverage
- 11 shore peak
- 12 shore srna
- 13 shore tagstats
- 14 shore structure
- 15 shore count
- 16 shore binom_test
- 17 shore mtc
- 18 shore ranksim
- 19 shore annotate_region
- 20 shore convert
- 21 shore sort
- 22 shore compress
- 23 shore 2dex
- 24 shore idtrans
shore preprocess
Prepares index files, local repeat and gc content files from reference sequence
shore import
Prepare short read data for processing
shore mapflowcell
Short read mapping
shore correct4pe
Improves mapping using paired-end information
shore merge
Merges and filters alignment files
shore mapview
Text-based alignment visualization
shore consensus
Creates consensus sequence from alignments (legacy version)
shore qVar
Computes consensus sequence, SNPs, indels and CNVs from alignments
shore methyl
Quantify methylated and unmethylated cytosines from BS-seq alignments (only genomemapper)
shore coverage
Coverage analysis and segmentation
shore peak
ChIP-seq peak detection
shore srna
Small RNA analysis
shore tagstats
Gather read statistics for multiple samples without a reference sequence
shore structure
Detect structural variants
shore count
Count reads
shore binom_test
Compares two sets of read counts using a binomial test
shore mtc
Generic multiple testing correction
shore ranksim
Rankproduct / ranksum simulator
shore annotate_region
Relate loci to annotation
shore convert
Convert SHORE files into common file formats, and vice versa
shore sort
Sort / merge tab-delimited text files
shore compress
Compress files to indexed gzip format
shore 2dex
Range-indexing and query for tab-delimited text files
shore idtrans
Translate SHORE sequence IDs into sequence names, and vice versa
