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C: Filtering out by gene and samples from VCF files
4.5 years ago by
gprashant17
▴ 110
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Comment:
C: Filtering significant somatic variants from a VCF file
4.8 years ago by
gprashant17
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Comment:
C: Empty VCF files produced by both Mutect2 and HaplotypeCaller?
updated 4.9 years ago by
Ram
43k • written 4.9 years ago by
gprashant17
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Comment:
C: Empty VCF files produced by both Mutect2 and HaplotypeCaller?
4.9 years ago by
gprashant17
▴ 110
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929
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Comment:
C: MarkDuplicates output file in GATK pipeline
4.9 years ago by
gprashant17
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4.0k
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Comment:
C: What are the best set of options to use while aligning using STAR?
4.9 years ago by
gprashant17
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Comment:
C: What are the best set of options to use while aligning using STAR?
4.9 years ago by
gprashant17
▴ 110
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908
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Comment:
C: What are the best tools for analyzing and identifying somatic mutations?
4.9 years ago by
gprashant17
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1.9k
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Comment:
C: Usage of Mutect2
4.9 years ago by
gprashant17
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3.1k
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Comment:
C: Viewing and editing FASTQ files
4.9 years ago by
gprashant17
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3.1k
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Comment:
C: Viewing and editing FASTQ files
4.9 years ago by
gprashant17
▴ 110
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3.1k
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Comment:
C: Viewing and editing FASTQ files
4.9 years ago by
gprashant17
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