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0
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Comment: Comment: conda error
8 months ago by svp ▴ 520
0
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1
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659
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Answer: Answer: conda error
8 months ago by svp ▴ 520
5
votes
2
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410
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Fastq: how can I check if they are from DNA or RNAseq data?
WES Fastq
updated 8 months ago by ★ 5.0k • written 8 months ago by ▴ 520
4
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0
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602
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Answer: A: Calling triovariants using varscan from a compressed mileup file ?
2.2 years ago by svp ▴ 520
0
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0
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1.7k
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Comment: C: Is anybody experiencing problems downloading from the SRA?
2.2 years ago by svp ▴ 520
2
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0
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1.9k
views
Comment: C: How to call denovo and rare variants from a trios cohort?
2.2 years ago by svp ▴ 520
3
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0
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770
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Comment: C: CalculateGenotypePosteriors: A USER ERROR has occurred: Invalid argument ' '.
2.2 years ago by svp ▴ 520
0
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0
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3.8k
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Comment: C: Combine two VCF files with GATK4
2.2 years ago by svp ▴ 520
3
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0
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3.8k
views
Answer: A: Combine two VCF files with GATK4
2.2 years ago by svp ▴ 520
4
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0
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1.0k
views
Comment: C: How do we deal with `MIXED` type variants in VQSR mode of Variant filtering ?
2.2 years ago by svp ▴ 520
0
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0
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3.6k
views
Comment: C: GATK4 VariantRecalibrator resource error
2.2 years ago by svp ▴ 520
1
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0
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623
views
Comment: C: How to call denovo variants from multiple trios cohort?
2.2 years ago by svp ▴ 520
4
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0
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45k
views
Answer: A: pheatmap: Error in hclust(d, method = method) : NA/NaN/Inf in foreign function
2.3 years ago by svp ▴ 520
3
votes
0
replies
6.5k
views
Answer: A: Generating heatmaps of pre-selected candidate genes after deseq2
2.3 years ago by svp ▴ 520
1
vote
0
replies
960
views
Comment: C: Access metadata in GEO expression datasets
2.4 years ago by svp ▴ 520
0
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0
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960
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Comment: C: Access metadata in GEO expression datasets
2.4 years ago by svp ▴ 520
1
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0
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796
views
Comment: C: Color code samples
2.5 years ago by svp ▴ 520
0
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0
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707
views
Comment: C: SNPs not filtered from a GATK vcf file
2.5 years ago by svp ▴ 520
3
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0
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1.0k
views
Answer: A: Web scraping in the KEGG db
2.5 years ago by svp ▴ 520
1
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0
replies
4.0k
views
Answer: A: RSEM Error - rsem-calculate-expression
2.5 years ago by svp ▴ 520
2
votes
1
reply
918
views
How to classify Tumor Mutation Burden into TMB high, medium and low groups ?
exome tumor mutation burden TMB
updated 2.5 years ago by ▴ 310 • written 2.5 years ago by ▴ 520
0
votes
1
reply
923
views
Does HaploypeCaller detects somatic mutations also?
HaplotypeCaller Mutation Exome somatic germline
updated 2.6 years ago by 47k • written 2.6 years ago by ▴ 520
6
votes
1
reply
1.7k
views
what is the difference between calling variants with and without interval list?
GATK HaplotypeCaller intervallist
updated 2.6 years ago by ▴ 110 • written 2.6 years ago by ▴ 520
0
votes
1
reply
478
views
How to interpret the values given in the BisoGenet output table ?
BisoGenet protein interction nework Cytoscape
updated 2.6 years ago by ▴ 600 • written 2.6 years ago by ▴ 520
1
vote
0
replies
525
views
How to extract list of proteins delectable by immune histochemistry?
Immune Histochemistry IHC detection cancer
2.6 years ago by svp ▴ 520
1
vote
0
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818
views
Comment: C: Calculation of Mentha Score
2.6 years ago by svp ▴ 520
2
votes
0
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793
views
Answer: A: How to perform batch correction when we have only single condition?
2.6 years ago by svp ▴ 520
5
votes
2
replies
793
views
How to perform batch correction when we have only single condition?
DESeq2 batcheffects sva combat
2.6 years ago by svp ▴ 520
0
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1
reply
3.9k
views
Comment: C: Normalization of RNASeq read counts without conditions
2.7 years ago by svp ▴ 520
6
votes
1
reply
1.2k
views
How can I call both somatic and germline variants from bam file?
exome variant calling somatic germline ngs
updated 2.7 years ago by ▴ 70 • written 2.7 years ago by ▴ 520
0
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1
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30k
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Answer: A: Converting a VCF with SNPs and indels to BED format
2.7 years ago by svp ▴ 520
0
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0
replies
813
views
Comment: C: Why snpEff annotates same region with different "effects" and why some effects a
2.8 years ago by svp ▴ 520
0
votes
1
reply
813
views
Comment: C: Why snpEff annotates same region with different "effects" and why some effects a
2.8 years ago by svp ▴ 520
0
votes
4
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813
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Why snpEff annotates same region with different "effects" and why some effects are given in combination? What is the criteria to filter this annotati…
snpEff VEP VariantAnnotation Exome VCF
2.8 years ago by svp ▴ 520
2
votes
1
reply
562
views
How to convert genomic region of following type to vcf file?
VCF Conversion LiftOver
updated 2.8 years ago by 153k • written 2.8 years ago by ▴ 520
5
votes
4
replies
5.7k
views
Why 'filterByExpr' does not eliminate low read counts from the expression data?
edgeR RNA-Seq DEGs filterByExpr
updated 2.8 years ago by ★ 5.6k • written 2.8 years ago by ▴ 520
3
votes
0
replies
2.0k
views
Answer: A: How do I run a .fastq single-end file in rsem-calculate-expression?
3.0 years ago by svp ▴ 520
3
votes
1
reply
2.2k
views
What is the difference of output samtools depth and samtools view -c on location of bam file?
samtools depth count bam
updated 3.0 years ago by ★ 1.0k • written 3.0 years ago by ▴ 520
1
vote
0
replies
812
views
Answer: A: How to get reference genome sequence given species name
3.0 years ago by svp ▴ 520
0
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0
replies
3.0k
views
Answer: A: depth calculation for targeted resequencing
3.0 years ago by svp ▴ 520
0
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0
replies
9.4k
views
Comment: C: Compute mean depth coverage for exome data with paired end, overlapping, feature
3.0 years ago by svp ▴ 520
0
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1
reply
9.4k
views
Comment: C: Compute mean depth coverage for exome data with paired end, overlapping, feature
3.0 years ago by svp ▴ 520
0
votes
1
reply
9.4k
views
Comment: C: Compute mean depth coverage for exome data with paired end, overlapping, feature
3.0 years ago by svp ▴ 520
0
votes
1
reply
214k
views
Comment: C: Tools To Calculate Average Coverage For A Bam File?
3.0 years ago by svp ▴ 520
0
votes
1
reply
610
views
How to extract coverage of custom target regions (bed file) from a bam file?
coverage bedtools
3.0 years ago by svp ▴ 520
1
vote
0
replies
27k
views
Comment: C: Bed For Agilent Sureselect All Exon Kits ?
3.1 years ago by svp ▴ 520
0
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0
replies
5.4k
views
Comment: C: CRAVAT: a web tool to annotate and analyze cancer variants
3.1 years ago by svp ▴ 520
1
vote
0
replies
4.5k
views
Answer: A: /bin/bash/ command not found
3.1 years ago by svp ▴ 520
1
vote
1
reply
908
views
Comment: C: Software for Gene ontology enrichment graph
3.1 years ago by svp ▴ 520
0
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1
reply
2.1k
views
Comment: C: How to filter fastq paired-end reads based on Per Tile Sequence Quality
3.2 years ago by svp ▴ 520
51 results • Page 1 of 2
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