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3.8k
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Comment:
A: vcf files in gatk not showing data lines
8.1 years ago by
H.Hasani
▴ 990
0
votes
0
replies
1.7k
views
Comment:
C: Help with looking at mutations from RNA-SEQ data
8.1 years ago by
H.Hasani
▴ 990
0
votes
0
replies
2.0k
views
Comment:
C: include indels along with SNPs in linear model
8.1 years ago by
H.Hasani
▴ 990
0
votes
0
replies
2.9k
views
Comment:
C: Are indel realignment and base recalibration necessary for RNAseq data?
8.1 years ago by
H.Hasani
▴ 990
0
votes
0
replies
2.3k
views
Comment:
C: How to convert gene names into ID symbol in NCBI
8.1 years ago by
H.Hasani
▴ 990
0
votes
1
reply
3.2k
views
Comment:
C: Calculate AB (allele balance) using SnpEff/SnpSift
8.1 years ago by
H.Hasani
▴ 990
0
votes
0
replies
2.6k
views
Answer:
A: Presenting "Role of genomics in cancer" to graduate students from different fiel
8.1 years ago by
H.Hasani
▴ 990
0
votes
0
replies
3.6k
views
Comment:
C: Extract Reads from a Sam file outside a given region
8.1 years ago by
H.Hasani
▴ 990
0
votes
1
reply
3.2k
views
Comment:
C: Calculate AB (allele balance) using SnpEff/SnpSift
8.1 years ago by
H.Hasani
▴ 990
0
votes
1
reply
1.9k
views
Answer:
A: ncRNAs with CDS in NCBI
8.2 years ago by
H.Hasani
▴ 990
0
votes
1
reply
1.9k
views
Comment:
C: ncRNAs with CDS in NCBI
8.2 years ago by
H.Hasani
▴ 990
0
votes
1
reply
2.3k
views
Answer:
A: How to convert gene names into ID symbol in NCBI
8.2 years ago by
H.Hasani
▴ 990
0
votes
0
replies
6.1k
views
Comment:
C: Obtaining bam files from ICGC or TCGC
8.2 years ago by
H.Hasani
▴ 990
1
vote
0
replies
3.1k
views
Comment:
C: GEOquery Problems to Get GEO dataset
8.2 years ago by
H.Hasani
▴ 990
0
votes
0
replies
7.5k
views
Comment:
C: Samtools Error Message, Please Help !
8.2 years ago by
H.Hasani
▴ 990
3
votes
11
replies
6.1k
views
Obtaining bam files from ICGC or TCGC
RNA-Seq
SNP
genome
updated 8.2 years ago by
Danielk
▴ 640 • written 8.2 years ago by
H.Hasani
▴ 990
0
votes
0
replies
6.1k
views
Comment:
C: Obtaining bam files from ICGC or TCGC
8.2 years ago by
H.Hasani
▴ 990
0
votes
0
replies
2.5k
views
Comment:
C: [cBioPortal] [GATK] [TCGA] Somatic variant calling error
8.2 years ago by
H.Hasani
▴ 990
0
votes
1
reply
6.1k
views
Comment:
C: Obtaining bam files from ICGC or TCGC
8.2 years ago by
H.Hasani
▴ 990
0
votes
1
reply
6.1k
views
Comment:
C: Obtaining bam files from ICGC or TCGC
8.2 years ago by
H.Hasani
▴ 990
0
votes
0
replies
7.5k
views
Comment:
C: What is the reason for most software errors in Bioinformatics according to you?
8.2 years ago by
H.Hasani
▴ 990
1
vote
0
replies
1.7k
views
Answer:
A: Genomic variation course at the EBI
8.2 years ago by
H.Hasani
▴ 990
0
votes
1
reply
4.3k
views
Answer:
A: Is reference genome same for DNA and RNA sequence alignment
8.2 years ago by
H.Hasani
▴ 990
0
votes
1
reply
2.8k
views
Answer:
A: Are there recommended steps if MuSiC reports too many significantly mutated gene
8.2 years ago by
H.Hasani
▴ 990
1
vote
0
replies
2.6k
views
Answer:
A: I'm in a Masters of Bioinformatics Program and wanted to ask everyone for advice
8.2 years ago by
H.Hasani
▴ 990
0
votes
1
reply
32k
views
Comment:
C: How to create a mutation landscape (waterfall) plot with GenVisR
8.2 years ago by
H.Hasani
▴ 990
0
votes
0
replies
2.3k
views
Comment:
C: Sanger sequencing results don't match the reference and alt alleles?
8.2 years ago by
H.Hasani
▴ 990
1
vote
0
replies
2.3k
views
Answer:
A: Sanger sequencing results don't match the reference and alt alleles?
8.2 years ago by
H.Hasani
▴ 990
1
vote
1
reply
4.6k
views
Answer:
A: Do I need to use hg19 or hg38 reference for performing variant calling analysis
8.2 years ago by
H.Hasani
▴ 990
1
vote
1
reply
2.4k
views
Comment:
C: NGS data analysis
8.2 years ago by
H.Hasani
▴ 990
1
vote
1
reply
2.4k
views
Comment:
C: Biostatistician's ability to work on NGS data analysis
8.2 years ago by
H.Hasani
▴ 990
0
votes
0
replies
4.2k
views
Comment:
C: Pipeline of structural variation calling using multiple tools for multiple sampl
8.2 years ago by
H.Hasani
▴ 990
3
votes
0
replies
3.6k
views
Comment:
C: How to find exact allele frequency for the SNP/indel variants ?
8.2 years ago by
H.Hasani
▴ 990
1
vote
1
reply
3.6k
views
Answer:
A: How to find exact allele frequency for the SNP/indel variants ?
8.2 years ago by
H.Hasani
▴ 990
1
vote
1
reply
7.7k
views
Comment:
C: Difference Between GATK, Freebayes and SAMtools mpileup
8.2 years ago by
H.Hasani
▴ 990
2
votes
0
replies
7.7k
views
Answer:
A: Difference Between GATK, Freebayes and SAMtools mpileup
8.2 years ago by
H.Hasani
▴ 990
0
votes
0
replies
3.1k
views
Comment:
Comment: MutSigCV-errors-Gene, patient, chr_file
updated 22 months ago by
Ram
44k • written 8.2 years ago by
H.Hasani
▴ 990
0
votes
0
replies
43k
views
Comment:
C: How To Create Mutation Diagram In R Or In Any Tools?
8.5 years ago by
H.Hasani
▴ 990
0
votes
0
replies
1.0k
views
Cancer mutations in Tumour and Tumour free
snp
rna-seq
updated 22 months ago by
Ram
44k • written 8.5 years ago by
H.Hasani
▴ 990
0
votes
0
replies
2.8k
views
Answer:
A: Allele frequencies in pedigrees
8.5 years ago by
H.Hasani
▴ 990
0
votes
1
reply
2.9k
views
Comment:
C: What is the reason for deviation from diagonal?
8.5 years ago by
H.Hasani
▴ 990
0
votes
2
replies
2.9k
views
Comment:
C: What is the reason for deviation from diagonal?
8.5 years ago by
H.Hasani
▴ 990
4
votes
0
replies
3.0k
views
Comment:
A: How many SNPs are sufficiant for covering?
8.5 years ago by
H.Hasani
▴ 990
2
votes
0
replies
2.9k
views
Answer:
A: SNP zygosity from RNA-Seq data (BAM file)
8.5 years ago by
H.Hasani
▴ 990
194 results • Page
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