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Answer: Answer: X chromosome male and female imputation
4 weeks ago by barslmn ★ 2.5k
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1
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7.5k
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Comment: Comment: Variant analysis for mouse WES
6 weeks ago by barslmn ★ 2.5k
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3
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6.9k
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Calculation variant frequencies for copy number events for a cohort
cnv vcf variant frequency
7 weeks ago by barslmn ★ 2.5k
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0
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6.9k
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Answer: Answer: Calculation variant frequencies for copy number events for a cohort
7 weeks ago by barslmn ★ 2.5k
2
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4.1k
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Answer: Answer: When to merge RNA-seq files with multiple sequencing lanes
8 weeks ago by barslmn ★ 2.5k
2
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0
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913
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Answer: Answer: custom BED to UCSC genome browser
4 months ago by barslmn ★ 2.5k
1
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2.8k
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Comment: Comment: Bioinformatics Docker Images Project (https://pegi3s.github.io/dockerfiles/)
6 months ago by barslmn ★ 2.5k
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1.5k
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Comment: Comment: Question about an alignment
7 months ago by barslmn ★ 2.5k
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0
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1.5k
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Comment: Comment: Question about an alignment
7 months ago by barslmn ★ 2.5k
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2
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1.5k
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Comment: Comment: Question about an alignment
7 months ago by barslmn ★ 2.5k
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10
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1.5k
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Question about an alignment
ces sequencing alignment
7 months ago by barslmn ★ 2.5k
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1.5k
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Comment: Comment: Question about an alignment
7 months ago by barslmn ★ 2.5k
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679
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Answer: Answer: Pipeline for Illumina GSAv3 in Beagle, ADMIXTURE and qpAdm?
11 months ago by barslmn ★ 2.5k
2
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0
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1.3k
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Answer: Answer: STAR alignment for RNA seq - trouble occurred
11 months ago by barslmn ★ 2.5k
1
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0
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972
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Comment: Comment: A notebook for checking relatedness and X heterozygosity from sequencing data
12 months ago by barslmn ★ 2.5k
4
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2
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972
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Tool: A notebook for checking relatedness and X heterozygosity from sequencing data
heterozygosity relatedness sequencing sex estimation
12 months ago by barslmn ★ 2.5k
0
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0
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772
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Answer: Answer: Minor Allele Frequency Calculation for 23andMe data
12 months ago by barslmn ★ 2.5k
1
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1
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4.2k
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Comment: Comment: How to improve a bioinformatics study and paper so that it is not considered "to
15 months ago by barslmn ★ 2.5k
1
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0
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5.1k
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Comment: Comment: Good Bioinformatics Jokes/Puns?
16 months ago by barslmn ★ 2.5k
2
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0
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569
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Blog: Investigating male X heterozygosity in short read sequencing
heterozygosity nextflow sequencing chrX
16 months ago by barslmn ★ 2.5k
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0
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2.0k
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Comment: Comment: Just released VEBA 2.0 in Nucleic Acids Research, a modular genome-resolved meta
16 months ago by barslmn ★ 2.5k
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0
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995
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Comment: Comment: HGNC Version Control
16 months ago by barslmn ★ 2.5k
6
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2
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995
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Tool: HGNC Version Control
git control symbols version gene
16 months ago by barslmn ★ 2.5k
1
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1
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1.3k
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Comment: Comment: QC Analysis from Sanger sequencing
17 months ago by barslmn ★ 2.5k
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0
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970
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Comment: Comment: Odd alignment question/finding
18 months ago by barslmn ★ 2.5k
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0
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1.5k
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Comment: Comment: AGeNT LocatIt
18 months ago by barslmn ★ 2.5k
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0
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2.9k
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Comment: Comment: Why multiple SYMBOLS, Consequences... for Variant Effect Predictor (VEP)
19 months ago by barslmn ★ 2.5k
0
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1
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2.9k
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Comment: Comment: Why multiple SYMBOLS, Consequences... for Variant Effect Predictor (VEP)
19 months ago by barslmn ★ 2.5k
4
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1
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1.2k
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Answer: Answer: Can questions and answers on biostars be asked only in English? Can't I use Russ
19 months ago by barslmn ★ 2.5k
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0
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2.6k
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Comment: Comment: Filtering VCF based on codon-transcript
19 months ago by barslmn ★ 2.5k
0
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1
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1.3k
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Answer: Answer: Development plan for a bioinformatics database developer/coder
19 months ago by barslmn ★ 2.5k
0
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1
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2.6k
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Comment: Comment: Filtering VCF based on codon-transcript
20 months ago by barslmn ★ 2.5k
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0
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1.8k
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Comment: Comment: I am trying to generate a bcf file through samtools mpileup but it taking too lo
20 months ago by barslmn ★ 2.5k
0
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2
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1.8k
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Comment: Comment: I am trying to generate a bcf file through samtools mpileup but it taking too lo
20 months ago by barslmn ★ 2.5k
0
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1
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2.6k
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Comment: Comment: Filtering VCF based on codon-transcript
20 months ago by barslmn ★ 2.5k
0
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0
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767
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Comment: Comment: VEP fail to annotate NCBI refseq GFF
20 months ago by barslmn ★ 2.5k
1
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0
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953
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Comment: Comment: VCF file transfer to a better genome
20 months ago by barslmn ★ 2.5k
0
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0
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6.9k
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Comment: Comment: Calculation variant frequencies for copy number events for a cohort
20 months ago by barslmn ★ 2.5k
0
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1
reply
2.6k
views
Comment: Comment: Filtering VCF based on codon-transcript
20 months ago by barslmn ★ 2.5k
1
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0
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3.1k
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Comment: Comment: Processing fastq files for genome assembly
20 months ago by barslmn ★ 2.5k
0
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1
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1.2k
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Comment: Comment: Issues with bcftools
20 months ago by barslmn ★ 2.5k
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0
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21k
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Comment: Comment: Issues installing bcl2fastq?
20 months ago by barslmn ★ 2.5k
1
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0
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21k
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Comment: Comment: Issues installing bcl2fastq?
updated 20 months ago by 45k • written 20 months ago by ★ 2.5k
0
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1
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2.6k
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Comment: Comment: Filtering VCF based on codon-transcript
updated 19 months ago by 45k • written 20 months ago by ★ 2.5k
1
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0
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1.6k
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Answer: Answer: Nextflow crash on AWS Batch with transition error
20 months ago by barslmn ★ 2.5k
1
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0
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1.3k
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Comment: Comment: Strategies with annotated VCF files to filter very big VCF from WGS
21 months ago by barslmn ★ 2.5k
1
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0
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1.5k
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Comment: Comment: Generate BED file
21 months ago by barslmn ★ 2.5k
0
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0
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2.2k
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Comment: Comment: Error message: "separator must begin with the '+' sign. cluster 1" during Fastq
21 months ago by barslmn ★ 2.5k
1
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0
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1.4k
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Answer: Answer: split sequences into their codons in a table
21 months ago by barslmn ★ 2.5k
1
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0
replies
1.2k
views
Comment: Comment: Re-format sample columns in VCF file
21 months ago by barslmn ★ 2.5k
362 results • Page 1 of 8
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