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2
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Comment: Comment: Calculation of TMB on gene level
7 months ago by svp ▴ 680
2
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1.1k
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Comment: Comment: Calculation of TMB on gene level
7 months ago by svp ▴ 680
3
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1
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1.1k
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Comment: Comment: Calculation of TMB on gene level
7 months ago by svp ▴ 680
0
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1
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1.6k
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Comment: Comment: conda error
21 months ago by svp ▴ 680
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2.6k
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Comment: C: Is anybody experiencing problems downloading from the SRA?
3.3 years ago by svp ▴ 680
2
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0
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2.8k
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Comment: C: How to call denovo and rare variants from a trios cohort?
3.3 years ago by svp ▴ 680
4
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1.2k
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Comment: C: CalculateGenotypePosteriors: A USER ERROR has occurred: Invalid argument ' '.
3.3 years ago by svp ▴ 680
0
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0
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6.1k
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Comment: C: Combine two VCF files with GATK4
3.3 years ago by svp ▴ 680
5
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1.6k
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Comment: C: How do we deal with `MIXED` type variants in VQSR mode of Variant filtering ?
3.3 years ago by svp ▴ 680
0
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0
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4.9k
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Comment: C: GATK4 VariantRecalibrator resource error
3.3 years ago by svp ▴ 680
1
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0
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926
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Comment: C: How to call denovo variants from multiple trios cohort?
3.3 years ago by svp ▴ 680
1
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0
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1.5k
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Comment: C: Access metadata in GEO expression datasets
3.5 years ago by svp ▴ 680
0
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1.5k
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Comment: C: Access metadata in GEO expression datasets
3.5 years ago by svp ▴ 680
1
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0
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1.0k
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Comment: C: Color code samples
3.6 years ago by svp ▴ 680
0
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0
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942
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Comment: C: SNPs not filtered from a GATK vcf file
3.6 years ago by svp ▴ 680
1
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0
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948
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Comment: C: Calculation of Mentha Score
3.7 years ago by svp ▴ 680
0
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1
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4.2k
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Comment: C: Normalization of RNASeq read counts without conditions
3.8 years ago by svp ▴ 680
0
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0
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1.1k
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Comment: C: Why snpEff annotates same region with different "effects" and why some effects a
3.9 years ago by svp ▴ 680
0
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1
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1.1k
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Comment: C: Why snpEff annotates same region with different "effects" and why some effects a
3.9 years ago by svp ▴ 680
0
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0
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12k
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Comment: C: Compute mean depth coverage for exome data with paired end, overlapping, feature
4.2 years ago by svp ▴ 680
0
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1
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12k
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Comment: C: Compute mean depth coverage for exome data with paired end, overlapping, feature
4.2 years ago by svp ▴ 680
0
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1
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12k
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Comment: C: Compute mean depth coverage for exome data with paired end, overlapping, feature
4.2 years ago by svp ▴ 680
0
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1
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239k
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Comment: C: Tools To Calculate Average Coverage For A Bam File?
4.2 years ago by svp ▴ 680
1
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0
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30k
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Comment: C: Bed For Agilent Sureselect All Exon Kits ?
4.2 years ago by svp ▴ 680
0
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0
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5.9k
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Comment: C: CRAVAT: a web tool to annotate and analyze cancer variants
4.2 years ago by svp ▴ 680
1
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1
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1.3k
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Comment: C: Software for Gene ontology enrichment graph
4.2 years ago by svp ▴ 680
0
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1
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2.5k
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Comment: C: How to filter fastq paired-end reads based on Per Tile Sequence Quality
4.3 years ago by svp ▴ 680
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