mapGL 1.0.0

Prediction of lineage-specific gain and loss of sequence elements using phylogenetic maximum parsimony.

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mapGL

Prediction of lineage-specific gain and loss of genomic sequence elements based on phylogenetic maximum parsimony.

Label genomic regions as orthologous, gained in the query species, or lost in the target species, based on inferred presence/absence in the most-recent common ancestor (MRCA). Chained alignment files are used to map features from query to target and one or more outgroup species. Features that map directly from query to target are labeled as orthologs, and ortholgous coordinates in the target species are given in the output. Non-mapping features are assigned as gains or losses based on a maximum-parsimony algorithm predicting presence or absence in the MRCA.

Based on bnMapper.py, by Ogert Denas (James Taylor lab):

• https://github.com/bxlab/bx-python/blob/master/scripts/bnMapper.py
• https://travis-ci.org/bxlab/bx-python

Dependencies

numpy bx-python cython six

Usage

mapGL.py [-h] [-o FILE] [-t FLOAT] [-g GAP] [-v {info,debug,silent}] [-k] input tree qname tname alignments [alignments ...]

Required Arguments

Argument	Description
input	Input regions to process. Should be in standard bed format. Only the first four bed fields will be used.
tree	Phylogenetic tree describing relationships of query and target species to outgroups. Must be in standard Newick format. Branch lengths are optional, and will be ignored.
qname	Name of the query species. Regions from this species will be mapped to target species coordinates.
tname	Name of the target species. Regions from the query species will be mapped to coordinates from this species.
alignments	Alignment files (.chain or .pkl): One for the target species and one per outgroup species. Files should be named according to the convention: qname.tname[...].chain.gz, where qname is the query species name and tname is the name of the target/outgroup species. Names used for qname and tname must match names used in the phylogenetic tree.

Options

Option	Description
-h, --help	Show help message and exit.
-o FILE, --output FILE	Output file. (default: stdout)
-t FLOAT, --threshold FLOAT	Mapping threshold i.e., (elem * threshold) <= mapped_elem (default: 0.0)
-g GAP, --gap GAP	Ignore elements with an insertion/deletion of this or bigger size. (default: -1)
-v {info,debug,silent}, --verbose {info,debug,silent}	Verbosity level (default: info)
-d, --drop_split	Follow the bnMapper convention of silently dropping elements that span multiple chains, rather than the liftOver mapping convention for split alignments: keep elements that span multiple chains and report the longest aligned segment. This is not recommended, as it may lead to spurious gain/loss predictions for orthologous elements that happen to be split across chains due to chromosomal rearrangements, etc... (default: False)
-i {BED,narrowPeak}, --in_format {BED,narrowPeak}	Input file format. (default: BED)
-f, --full_labels	Predict gain/loss events on the whole tree, not just branches leading to query and target species. (default: False)

Output

Predictions are reported in tab-delimited format with the first four columns following the BED4 convention. The predicted evolutionary history (i.e., ortholog, gain in query, or loss in target) is reported in the "status" column. The final three columns contain the mapped location, in target coordinates, of mapped (ortholog) elements.

Column	Description
chrom	Chromosome on which the query element is located.
start	Start position on query chromosome.
end	End position on query chromosome.
name	Element name or ID.
peak	Peak location (narrowPeak input) or element midpoint (BED input)
status	Predicted phylogenetic history: ortholog, gain_qname, or loss_tname. If --full_labels is used, this may include additional loss/gain events on other branches, in a comma-delimited list format.
mapped chrom	For mapped (ortholog) elements, the chromosome on which the mapped element is located, in target coordinates.
mapped start	For mapped (ortholog) elements, the start position on the target chromosome on which the mapped element is located.
mapped end	For mapped (ortholog) elements, the end position on the target chromosome on which the mapped element is located.
mapped_peak	For mapped (ortholog) elements, the mapped peak position (narrowPeak input) or mapped element midpoint (BED input).

Copyright 2018, Adam Diehl ([e-mail]), Boyle Lab, University of Michigan