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3
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14k
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Comment: C: Determine sex from vcf file (or sequencing data)
9.5 years ago by H.Hasani ★ 1.0k
0
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0
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15k
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Answer: Answer: Map genetic mutations to protein domain/structure
updated 3.6 years ago by 45k • written 9.5 years ago by ★ 1.0k
0
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0
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3.5k
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Comment: C: How to Specify Genome Build in MutSigCV Input ?
9.6 years ago by H.Hasani ★ 1.0k
0
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0
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2.8k
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Comment: C: ORF search gives negative start value
9.6 years ago by H.Hasani ★ 1.0k
0
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0
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4.8k
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Comment: A: vcf files in gatk not showing data lines
9.6 years ago by H.Hasani ★ 1.0k
0
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0
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2.1k
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Comment: C: Help with looking at mutations from RNA-SEQ data
9.6 years ago by H.Hasani ★ 1.0k
0
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0
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2.3k
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Comment: C: include indels along with SNPs in linear model
9.6 years ago by H.Hasani ★ 1.0k
0
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0
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3.5k
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Comment: C: Are indel realignment and base recalibration necessary for RNAseq data?
9.6 years ago by H.Hasani ★ 1.0k
0
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0
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2.7k
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Comment: C: How to convert gene names into ID symbol in NCBI
9.6 years ago by H.Hasani ★ 1.0k
0
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1
reply
3.8k
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Comment: C: Calculate AB (allele balance) using SnpEff/SnpSift
9.6 years ago by H.Hasani ★ 1.0k
0
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0
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3.4k
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Answer: A: Presenting "Role of genomics in cancer" to graduate students from different fiel
9.6 years ago by H.Hasani ★ 1.0k
0
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0
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4.4k
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Comment: C: Extract Reads from a Sam file outside a given region
9.6 years ago by H.Hasani ★ 1.0k
0
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1
reply
3.8k
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Comment: C: Calculate AB (allele balance) using SnpEff/SnpSift
9.6 years ago by H.Hasani ★ 1.0k
0
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1
reply
2.4k
views
Answer: A: ncRNAs with CDS in NCBI
9.6 years ago by H.Hasani ★ 1.0k
0
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1
reply
2.4k
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Comment: C: ncRNAs with CDS in NCBI
9.6 years ago by H.Hasani ★ 1.0k
0
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1
reply
2.7k
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Answer: A: How to convert gene names into ID symbol in NCBI
9.6 years ago by H.Hasani ★ 1.0k
0
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0
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7.8k
views
Comment: C: Obtaining bam files from ICGC or TCGC
9.6 years ago by H.Hasani ★ 1.0k
1
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0
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3.6k
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Comment: C: GEOquery Problems to Get GEO dataset
9.6 years ago by H.Hasani ★ 1.0k
0
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0
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8.4k
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Comment: C: Samtools Error Message, Please Help !
9.6 years ago by H.Hasani ★ 1.0k
3
votes
11
replies
7.8k
views
Obtaining bam files from ICGC or TCGC
RNA-Seq SNP genome
updated 9.6 years ago by ▴ 640 • written 9.6 years ago by ★ 1.0k
0
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0
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7.8k
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Comment: C: Obtaining bam files from ICGC or TCGC
9.6 years ago by H.Hasani ★ 1.0k
0
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0
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2.8k
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Comment: C: [cBioPortal] [GATK] [TCGA] Somatic variant calling error
9.6 years ago by H.Hasani ★ 1.0k
0
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1
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7.8k
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Comment: C: Obtaining bam files from ICGC or TCGC
9.6 years ago by H.Hasani ★ 1.0k
0
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1
reply
7.8k
views
Comment: C: Obtaining bam files from ICGC or TCGC
9.6 years ago by H.Hasani ★ 1.0k
0
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0
replies
10k
views
Comment: C: What is the reason for most software errors in Bioinformatics according to you?
9.6 years ago by H.Hasani ★ 1.0k
1
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0
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2.2k
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Answer: A: Genomic variation course at the EBI
9.6 years ago by H.Hasani ★ 1.0k
0
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1
reply
5.8k
views
Answer: A: Is reference genome same for DNA and RNA sequence alignment
9.6 years ago by H.Hasani ★ 1.0k
0
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1
reply
4.0k
views
Answer: A: Are there recommended steps if MuSiC reports too many significantly mutated gene
9.6 years ago by H.Hasani ★ 1.0k
1
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0
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3.8k
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Answer: A: I'm in a Masters of Bioinformatics Program and wanted to ask everyone for advice
9.6 years ago by H.Hasani ★ 1.0k
0
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1
reply
37k
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Comment: C: How to create a mutation landscape (waterfall) plot with GenVisR
9.7 years ago by H.Hasani ★ 1.0k
0
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0
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3.3k
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Comment: C: Sanger sequencing results don't match the reference and alt alleles?
9.7 years ago by H.Hasani ★ 1.0k
1
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0
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3.3k
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Answer: A: Sanger sequencing results don't match the reference and alt alleles?
9.7 years ago by H.Hasani ★ 1.0k
1
vote
1
reply
5.8k
views
Answer: A: Do I need to use hg19 or hg38 reference for performing variant calling analysis
9.7 years ago by H.Hasani ★ 1.0k
1
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1
reply
3.2k
views
Comment: C: NGS data analysis
9.7 years ago by H.Hasani ★ 1.0k
1
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1
reply
3.2k
views
Comment: C: Biostatistician's ability to work on NGS data analysis
9.7 years ago by H.Hasani ★ 1.0k
0
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0
replies
4.8k
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Comment: C: Pipeline of structural variation calling using multiple tools for multiple sampl
9.7 years ago by H.Hasani ★ 1.0k
3
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0
replies
4.3k
views
Comment: C: How to find exact allele frequency for the SNP/indel variants ?
9.7 years ago by H.Hasani ★ 1.0k
1
vote
1
reply
4.3k
views
Answer: A: How to find exact allele frequency for the SNP/indel variants ?
9.7 years ago by H.Hasani ★ 1.0k
1
vote
1
reply
9.2k
views
Comment: C: Difference Between GATK, Freebayes and SAMtools mpileup
9.7 years ago by H.Hasani ★ 1.0k
2
votes
0
replies
9.2k
views
Answer: A: Difference Between GATK, Freebayes and SAMtools mpileup
9.7 years ago by H.Hasani ★ 1.0k
0
votes
0
replies
3.4k
views
Comment: Comment: MutSigCV-errors-Gene, patient, chr_file
updated 3.3 years ago by 45k • written 9.7 years ago by ★ 1.0k
0
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0
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49k
views
Comment: C: How To Create Mutation Diagram In R Or In Any Tools?
9.9 years ago by H.Hasani ★ 1.0k
0
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0
replies
1.2k
views
Cancer mutations in Tumour and Tumour free
snp rna-seq
updated 3.3 years ago by 45k • written 9.9 years ago by ★ 1.0k
0
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0
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3.5k
views
Answer: A: Allele frequencies in pedigrees
9.9 years ago by H.Hasani ★ 1.0k
0
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1
reply
3.9k
views
Comment: C: What is the reason for deviation from diagonal?
9.9 years ago by H.Hasani ★ 1.0k
0
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2
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3.9k
views
Comment: C: What is the reason for deviation from diagonal?
9.9 years ago by H.Hasani ★ 1.0k
4
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0
replies
3.6k
views
Comment: A: How many SNPs are sufficiant for covering?
9.9 years ago by H.Hasani ★ 1.0k
2
votes
0
replies
3.5k
views
Answer: A: SNP zygosity from RNA-Seq data (BAM file)
10.0 years ago by H.Hasani ★ 1.0k
198 results • Page 4 of 4
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