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Showing :
answers
2
votes
0
replies
2.4k
views
Answer:
Answer: Filtering long indels from VCF
8 months ago by
bari.ballew
▴ 460
0
votes
0
replies
910
views
Answer:
A: Genotyping samples at a predetermined list of locations
3.7 years ago by
bari.ballew
▴ 460
1
vote
0
replies
4.4k
views
Answer:
A: GATK GenomicsDBImport - use list as input
3.7 years ago by
bari.ballew
▴ 460
1
vote
1
reply
2.9k
views
Answer:
A: Rename Chromosome position/Notation in VCF file
4.0 years ago by
bari.ballew
▴ 460
2
votes
0
replies
983
views
Answer:
A: Identifying zygosity of somatic deletion
4.2 years ago by
bari.ballew
▴ 460
0
votes
0
replies
1.5k
views
Answer:
A: Are there any issues with using sample reads coming from different technologies
4.2 years ago by
bari.ballew
▴ 460
0
votes
0
replies
1.3k
views
Answer:
A: Selecting set of SNPs using vcftools
4.6 years ago by
bari.ballew
▴ 460
1
vote
0
replies
3.7k
views
Answer:
A: Snakemake FastQC MissingOutputFiles ErrorM
4.6 years ago by
bari.ballew
▴ 460
0
votes
1
reply
975
views
Answer:
A: Query regarding somatic variant calling
4.7 years ago by
bari.ballew
▴ 460
0
votes
0
replies
2.1k
views
Answer:
A: Removing white space from the beginning of the second field (sequence) in a fast
4.7 years ago by
bari.ballew
▴ 460
2
votes
0
replies
744
views
Answer:
A: Not call some variants in some populations?
4.7 years ago by
bari.ballew
▴ 460
0
votes
0
replies
884
views
Answer:
A: Merging SNV and DIV vcfs of the same Individual
4.7 years ago by
bari.ballew
▴ 460
3
votes
1
reply
1.4k
views
Answer:
A: skipping column names using awk
4.7 years ago by
bari.ballew
▴ 460
4
votes
1
reply
26k
views
Answer:
A: Best way to query VCF for specific variants
4.8 years ago by
bari.ballew
▴ 460
18
votes
1
reply
19k
views
Answer:
A: VCF merge or concatenate?
4.8 years ago by
bari.ballew
▴ 460
0
votes
0
replies
1.8k
views
Answer:
A: Filter out low coverage and minor alleles of a frequency above 40%.
4.8 years ago by
bari.ballew
▴ 460
0
votes
0
replies
1.3k
views
Answer:
A: Read .sample file (file format available in plink) as a dataframe in pandas
4.8 years ago by
bari.ballew
▴ 460
0
votes
0
replies
1.1k
views
Answer:
A: Matching mutation in bed files to their corresponding bam files
4.8 years ago by
bari.ballew
▴ 460
1
vote
0
replies
1.9k
views
Answer:
A: DeepVariant and Gene Panels
4.8 years ago by
bari.ballew
▴ 460
0
votes
0
replies
2.1k
views
Answer:
A: targets in a bed at or above a coverage
4.8 years ago by
bari.ballew
▴ 460
2
votes
0
replies
3.7k
views
Answer:
A: snakemake wildcard for fastq files
4.9 years ago by
bari.ballew
▴ 460
3
votes
0
replies
3.2k
views
Answer:
A: Rename FASTA headers based on filename
5.0 years ago by
bari.ballew
▴ 460
0
votes
1
reply
2.2k
views
Answer:
A: MAF file having mutation data
5.1 years ago by
bari.ballew
▴ 460
1
vote
0
replies
4.1k
views
Answer:
A: Downstream analysis of VCF files obtained from VarScan2
5.1 years ago by
bari.ballew
▴ 460
4
votes
0
replies
2.1k
views
Answer:
A: tool to detect large deletions
5.1 years ago by
bari.ballew
▴ 460
1
vote
1
reply
1.8k
views
Answer:
A: From pooled fastq data to SNPs
6.3 years ago by
bari.ballew
▴ 460
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