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enable rev-comp to deal with indel alleles (esp when using MASHR dbs) #37

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enable rev-comp to deal with indel alleles (esp when using MASHR dbs) #37

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8 changes: 6 additions & 2 deletions Software/PrediXcan.py
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Original file line number Diff line number Diff line change
Expand Up @@ -87,8 +87,12 @@ def __init__(self, beta_file, sample_file, gene_file=None):
self.beta_file = beta_file
self.gene_file = gene_file
self.sample_file = sample_file
self.complements = {"A":"T","C":"G","G":"C","T":"A"}
# self.complements = {"A":"T","C":"G","G":"C","T":"A"}

def reverse_complement(self,seq):
complement = {"A":"T","C":"G","G":"C","T":"A"}
reversedseq = "".join(complement.get(base, base) for base in reversed(seq))
return reversedseq
def get_gene_list(self):
if self.gene_file:
return list(sorted([line.strip().split()[-1] for line in open(self.gene_file)]))
Expand All @@ -101,7 +105,7 @@ def update(self, gene, weight, ref_allele, allele, dosage_row):
self.gene_index = { gene:k for (k, gene) in enumerate(self.gene_list) }
self.D = np.zeros((len(self.gene_list), len(dosage_row))) # Genes x Cases
if gene in self.gene_index: #assumes dosage coding 0 to 2
if ref_allele == allele or self.complements[ref_allele] == allele: # assumes non-ambiguous SNPs to resolve strand issues:
if ref_allele == allele or self.reverse_complement(ref_allele) == allele: # assumes non-ambiguous SNPs to resolve strand issues:
self.D[self.gene_index[gene],] += dosage_row * weight
else:
self.D[self.gene_index[gene],] += (2-dosage_row) * weight # Update all cases for that gene
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