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Eric Kofman
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Original file line number | Diff line number | Diff line change |
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# This sample has an edit at the very end of the read. It's a good test to ensure that we don't have off by one errors | ||
# in computing the coverage. It was aligned to the craig venter genome, so the reference is slightly difference from | ||
# hg38 -- if aligning with hg38, this read doesn't have mutations at these positions. | ||
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# Expected edit | ||
# AAACGAATCATTCATC-1 10_AAACGAATCATTCATC-1 10_AAACGAATCATTCATC-1:132330481 132330481 T G A00621:106:HLFHGDSXX:3:1152:16830:27352 - | ||
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# Expected combined.bed file | ||
# 10_AAACGAATCATTCATC-1 132330438 132330439 | ||
# 10_AAACGAATCATTCATC-1 132330481 132330482 | ||
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# Read | ||
# A00621:106:HLFHGDSXX:3:1152:16830:27352 16 10_AAACGAATCATTCATC-1 132330391 255 91M * 0 0 GCAACACCCATGTCACTCCTCATTCTCTCCTTGCTCTGCCCGGGTGGCTGGCCTCCCCACGCTCCTGAGAAGGTACTGGTTGTGCTTTCAG FFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFFF NH:i:1 HI:i:1 AS:i:89 nM:i:0 TX:Z:ENST00000456004,+406,91M GX:Z:ENSG00000165752 GN:Z:STK32C fx:Z:ENSG00000165752 RE:A:E li:i:0 BC:Z:TTTCCACT QT:Z:FFFFF:FF CR:Z:AAACGAATCATTCATC CY:Z:FFFFFFFFFFFFFFFF CB:Z:AAACGAATCATTCATC-1 UR:Z:CGCTTAAAACCT UY:Z:FFFFFFFFFFFF UB:Z:CGCTTAAAACCT xf:i:25 RG:Z:10X214_1_AB_1:0:1:HLFHGDSXX:3 NM:i:2 MD:Z:47T42T0 | ||
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mypython=$1 | ||
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$mypython $MARINE/marine.py \ | ||
--bam_filepath \ | ||
$MARINE/tests/singlecell_tests/bams/10_C-1_orig.bam \ | ||
--annotation_bedfile_path \ | ||
$MARINE/annotations/cellranger-GRCh38-3.0.0.annotation.genes.bed \ | ||
--output_folder \ | ||
$MARINE/tests/singlecell_tests/edge_case_test \ | ||
--min_base_quality \ | ||
15 \ | ||
--cores \ | ||
4 \ | ||
--barcode_tag "CB" \ | ||
--strandedness 2 --num_per_sublist 1 --verbose \ | ||
--contigs 10 --interval_length 40000000 --keep_intermediate_files |