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1
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6
replies
6.3k
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Mouse to Human Protein Alignment Maps
alignment sequence mouse
updated 20 months ago by ▴ 30 • written 9.1 years ago by ▴ 620
0
votes
0
replies
505
views
Reference Panel for Copy Number Analysis Based on Clinical Target Capture Sequencing
copynumber target-capture
2.4 years ago by Noushin N ▴ 620
1
vote
0
replies
3.4k
views
Comment: C: Ensembl REST API Optional Parameters
5.8 years ago by Noushin N ▴ 620
0
votes
0
replies
2.8k
views
Comment: C: Calling CNA from aCGH: Thresholding?
updated 5.8 years ago by 45k • written 9.8 years ago by ▴ 620
6
votes
6
replies
3.4k
views
Ensembl REST API Optional Parameters
ensembl VEP
updated 3.3 years ago by ★ 2.4k • written 5.8 years ago by ▴ 620
0
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0
replies
3.4k
views
Comment: C: Ensembl REST API Optional Parameters
5.8 years ago by Noushin N ▴ 620
0
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0
replies
1.5k
views
Comment: C: Rsamtools mpileup discrepancy
5.8 years ago by Noushin N ▴ 620
0
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2
replies
1.5k
views
Rsamtools mpileup discrepancy
samtools R
5.8 years ago by Noushin N ▴ 620
0
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0
replies
1.4k
views
Comment: C: Annotation with Ensembl REST API
5.9 years ago by Noushin N ▴ 620
0
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3
replies
1.4k
views
Annotation with Ensembl REST API
ensembl R API
updated 5.9 years ago by 24k • written 5.9 years ago by ▴ 620
0
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0
replies
1.4k
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Comment: C: Annotation with Ensembl REST API
5.9 years ago by Noushin N ▴ 620
0
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1
reply
12k
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Comment: C: Samtools Index Segmentation Fault
updated 6.1 years ago by 45k • written 11.6 years ago by ▴ 620
0
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0
replies
986
views
Intra-tumor Heterogeneity / Mutation Cellular Fraction in TCGA Data
TCGA Heterogeneity
6.8 years ago by Noushin N ▴ 620
0
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1
reply
2.0k
views
Array CGH quality control
array-cgh
updated 7.1 years ago by 89k • written 9.7 years ago by ▴ 620
2
votes
0
replies
2.6k
views
Answer: A: Mapability index (track) from UCSC
updated 7.2 years ago by 45k • written 9.7 years ago by ▴ 620
1
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1
reply
3.4k
views
Answer: A: using vcftools to add gene name to vcf file
updated 7.2 years ago by 45k • written 9.7 years ago by ▴ 620
0
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0
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2.2k
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Comment: A: How to find patient sample.type in TCGA-PRAD ?
7.4 years ago by Noushin N ▴ 620
1
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0
replies
2.5k
views
Answer: A: Inconsistency of allele depth in BAM and VCF
7.5 years ago by Noushin N ▴ 620
0
votes
0
replies
1.9k
views
Comment: C: Why GWASs cannot speculate what kind of mutation the SNP would cause?
7.7 years ago by Noushin N ▴ 620
5
votes
0
replies
1.9k
views
Answer: A: identifying TP53 germline mutations which are also in tumor cells.
7.7 years ago by Noushin N ▴ 620
2
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0
replies
1.4k
views
Answer: A: Is it possible to check whether a sample is progeny of the other two samples fro
7.8 years ago by Noushin N ▴ 620
2
votes
1
reply
1.9k
views
Answer: A: Why GWASs cannot speculate what kind of mutation the SNP would cause?
7.8 years ago by Noushin N ▴ 620
1
vote
0
replies
2.3k
views
Answer: A: Changing Chromosome Notation in Bam Files to Include Sample ID
7.8 years ago by Noushin N ▴ 620
1
vote
1
reply
44k
views
Answer: A: Remove columns and rows which have only NAs without deleting all the data
8.3 years ago by Noushin N ▴ 620
0
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0
replies
3.0k
views
Answer: A: retrieve genomic coordinate on mRNA
8.4 years ago by Noushin N ▴ 620
0
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0
replies
4.8k
views
Comment: C: B Allele Frequency (VAF) Segmentation Analysis
8.7 years ago by Noushin N ▴ 620
1
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1
reply
2.5k
views
Comment: C: Where is the BigWig Supplementary Information?
8.7 years ago by Noushin N ▴ 620
0
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1
reply
3.0k
views
Comment: C: Understanding coverage command
8.8 years ago by Noushin N ▴ 620
0
votes
0
replies
1.9k
views
Answer: A: is there any R package to measure the efficiency of different exome capture kits
8.8 years ago by Noushin N ▴ 620
0
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2
replies
5.8k
views
Comment: C: How to extract FORMAT information (GT, PG, PI, etc) from each SAMPLE in a vcf fi
8.8 years ago by Noushin N ▴ 620
0
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1
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5.8k
views
Comment: C: How to extract FORMAT information (GT, PG, PI, etc) from each SAMPLE in a vcf fi
8.8 years ago by Noushin N ▴ 620
1
vote
2
replies
5.8k
views
Answer: A: How to extract FORMAT information (GT, PG, PI, etc) from each SAMPLE in a vcf fi
8.8 years ago by Noushin N ▴ 620
2
votes
0
replies
8.3k
views
Answer: A: Benjamin Hochberg adjust P-values
8.9 years ago by Noushin N ▴ 620
1
vote
1
reply
25k
views
Comment: C: Calculating Variant Allele Frequency
8.9 years ago by Noushin N ▴ 620
2
votes
1
reply
25k
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Comment: C: Calculating Variant Allele Frequency
8.9 years ago by Noushin N ▴ 620
6
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1
reply
25k
views
Answer: A: Calculating Variant Allele Frequency
8.9 years ago by Noushin N ▴ 620
0
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1
reply
2.4k
views
Answer: A: Does ADTEx use CBS for segmentation?
9.0 years ago by Noushin N ▴ 620
0
votes
1
reply
3.7k
views
Answer: A: What the x-axis of this box plot is measuring?
9.0 years ago by Noushin N ▴ 620
1
vote
1
reply
3.3k
views
Comment: C: how to extract some probes from a file contains duplicated row names
9.0 years ago by Noushin N ▴ 620
1
vote
1
reply
3.3k
views
Answer: A: how to extract some probes from a file contains duplicated row names
9.0 years ago by Noushin N ▴ 620
0
votes
1
reply
6.3k
views
Comment: C: Mouse to Human Protein Alignment Maps
9.1 years ago by Noushin N ▴ 620
3
votes
1
reply
3.9k
views
Answer: A: Extract allele frequencies from VCF
9.2 years ago by Noushin N ▴ 620
1
vote
0
replies
2.1k
views
Comment: C: extract a table a subset from table
9.2 years ago by Noushin N ▴ 620
1
vote
0
replies
1.9k
views
Answer: A: Cancer DNA sequences
9.2 years ago by Noushin N ▴ 620
0
votes
1
reply
4.1k
views
Answer: A: SnpEff html result
9.2 years ago by Noushin N ▴ 620
0
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0
replies
2.0k
views
Comment: C: R script/package to plot mutation comparision in cancers
9.2 years ago by Noushin N ▴ 620
2
votes
1
reply
10k
views
Answer: A: Allele frequency of vcf file
9.2 years ago by Noushin N ▴ 620
6
votes
10
replies
5.2k
views
Somatic Mutation Phasing
cancer somatic haplotype
updated 9.2 years ago by 12k • written 11.8 years ago by ▴ 620
2
votes
1
reply
6.0k
views
Comment: C: Allele count for SNPs
9.3 years ago by Noushin N ▴ 620
7
votes
8
replies
8.4k
views
Parsing Base String From Samtools Mpileup
samtools mpileup
updated 4.0 years ago by 45k • written 12.3 years ago by ▴ 620
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