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C: GATK GenomicsDBImport - use list as input
3.8 years ago by
bari.ballew
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C: illumina variant interpreter vcf format version error
4.1 years ago by
bari.ballew
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A: MutSig2CV with self-generated "maf file:
4.8 years ago by
bari.ballew
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A: Filter out low coverage and minor alleles of a frequency above 40%.
4.9 years ago by
bari.ballew
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C: varscan tool for copy number variation detection
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C: Looking For Approaches For Finding Contamination And Sample Identity Matching Is
5.0 years ago by
bari.ballew
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C: MAF file having mutation data
5.1 years ago by
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C: MAF file having mutation data
5.1 years ago by
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