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Comment: Comment: A notebook for checking relatedness and X heterozygosity from sequencing data
14 days ago by barslmn ★ 2.3k
4
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2
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442
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Tool: A notebook for checking relatedness and X heterozygosity from sequencing data
heterozygosity relatedness sequencing sex estimation
14 days ago by barslmn ★ 2.3k
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0
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278
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Answer: Answer: Minor Allele Frequency Calculation for 23andMe data
22 days ago by barslmn ★ 2.3k
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1.2k
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Comment: Comment: How to improve a bioinformatics study and paper so that it is not considered "to
4 months ago by barslmn ★ 2.3k
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1.8k
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Comment: Comment: Good Bioinformatics Jokes/Puns?
4 months ago by barslmn ★ 2.3k
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0
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210
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Blog: Investigating male X heterozygosity in short read sequencing
heterozygosity nextflow sequencing chrX
4 months ago by barslmn ★ 2.3k
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0
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609
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Comment: Comment: Just released VEBA 2.0 in Nucleic Acids Research, a modular genome-resolved meta
4 months ago by barslmn ★ 2.3k
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0
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404
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Comment: Comment: HGNC Version Control
4 months ago by barslmn ★ 2.3k
6
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2
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404
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Tool: HGNC Version Control
git control symbols version gene
4 months ago by barslmn ★ 2.3k
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1
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583
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Comment: Comment: QC Analysis from Sanger sequencing
5 months ago by barslmn ★ 2.3k
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483
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Comment: Comment: Odd alignment question/finding
6 months ago by barslmn ★ 2.3k
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1.0k
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Comment: Comment: AGeNT LocatIt
7 months ago by barslmn ★ 2.3k
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1.5k
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Comment: Comment: Why multiple SYMBOLS, Consequences... for Variant Effect Predictor (VEP)
8 months ago by barslmn ★ 2.3k
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1
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1.5k
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Comment: Comment: Why multiple SYMBOLS, Consequences... for Variant Effect Predictor (VEP)
8 months ago by barslmn ★ 2.3k
4
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1
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588
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Answer: Answer: Can questions and answers on biostars be asked only in English? Can't I use Russ
8 months ago by barslmn ★ 2.3k
0
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0
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1.3k
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Comment: Comment: Filtering VCF based on codon-transcript
8 months ago by barslmn ★ 2.3k
0
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1
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718
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Answer: Answer: Development plan for a bioinformatics database developer/coder
8 months ago by barslmn ★ 2.3k
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1
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1.3k
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Comment: Comment: Filtering VCF based on codon-transcript
8 months ago by barslmn ★ 2.3k
0
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0
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987
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Comment: Comment: I am trying to generate a bcf file through samtools mpileup but it taking too lo
8 months ago by barslmn ★ 2.3k
0
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2
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987
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Comment: Comment: I am trying to generate a bcf file through samtools mpileup but it taking too lo
8 months ago by barslmn ★ 2.3k
0
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1
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1.3k
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Comment: Comment: Filtering VCF based on codon-transcript
8 months ago by barslmn ★ 2.3k
0
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0
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364
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Comment: Comment: VEP fail to annotate NCBI refseq GFF
8 months ago by barslmn ★ 2.3k
1
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489
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Comment: Comment: VCF file transfer to a better genome
8 months ago by barslmn ★ 2.3k
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0
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500
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Comment: Comment: Calculation variant frequencies for copy number events for a cohort
8 months ago by barslmn ★ 2.3k
2
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2
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500
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Calculation variant frequencies for copy number events for a cohort
cnv vcf variant frequency
8 months ago by barslmn ★ 2.3k
0
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1
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1.3k
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Comment: Comment: Filtering VCF based on codon-transcript
8 months ago by barslmn ★ 2.3k
1
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0
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1.6k
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Comment: Comment: Processing fastq files for genome assembly
8 months ago by barslmn ★ 2.3k
0
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1
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622
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Comment: Comment: Issues with bcftools
8 months ago by barslmn ★ 2.3k
0
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0
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17k
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Comment: Comment: Issues installing bcl2fastq?
8 months ago by barslmn ★ 2.3k
1
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0
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17k
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Comment: Comment: Issues installing bcl2fastq?
updated 8 months ago by 44k • written 8 months ago by ★ 2.3k
0
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1
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1.3k
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Comment: Comment: Filtering VCF based on codon-transcript
updated 8 months ago by 44k • written 8 months ago by ★ 2.3k
1
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0
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693
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Answer: Answer: Nextflow crash on AWS Batch with transition error
8 months ago by barslmn ★ 2.3k
1
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0
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734
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Comment: Comment: Strategies with annotated VCF files to filter very big VCF from WGS
9 months ago by barslmn ★ 2.3k
1
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0
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828
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Comment: Comment: Generate BED file
9 months ago by barslmn ★ 2.3k
0
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0
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1.6k
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Comment: Comment: Error message: "separator must begin with the '+' sign. cluster 1" during Fastq
9 months ago by barslmn ★ 2.3k
1
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0
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773
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Answer: Answer: split sequences into their codons in a table
10 months ago by barslmn ★ 2.3k
1
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0
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706
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Comment: Comment: Re-format sample columns in VCF file
10 months ago by barslmn ★ 2.3k
1
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0
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865
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Comment: Comment: NF-Core
10 months ago by barslmn ★ 2.3k
0
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0
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962
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Comment: Comment: Can I remove all variants in a vcf file that have 0/0 for PRS calculation?
10 months ago by barslmn ★ 2.3k
0
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0
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1.2k
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Answer: Answer: How to rename multiple fasq files
11 months ago by barslmn ★ 2.3k
2
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0
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503
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Comment: Comment: unicycler error : [Errno 13] Permission denied:
11 months ago by barslmn ★ 2.3k
0
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0
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411
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Comment: Comment: Python function to export the annotated records to genbank file using python and
11 months ago by barslmn ★ 2.3k
0
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1
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882
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Answer: Answer: AlphaMissense_hg38.tsv.gz tabix indexing issue VEP
12 months ago by barslmn ★ 2.3k
0
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0
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1.9k
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Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
12 months ago by barslmn ★ 2.3k
0
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1
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1.9k
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Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
12 months ago by barslmn ★ 2.3k
0
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1
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1.9k
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Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
12 months ago by barslmn ★ 2.3k
0
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1
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1.2k
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Comment: Comment: help with weird PCA? (vcfR)
12 months ago by barslmn ★ 2.3k
0
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1
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1.9k
views
Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
12 months ago by barslmn ★ 2.3k
1
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1
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1.9k
views
Answer: Answer: Locally annotating SNP IDs and Gene names of called variants
12 months ago by barslmn ★ 2.3k
0
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1
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1.2k
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Comment: Comment: help with weird PCA? (vcftools, Rstudio (vcfR)
12 months ago by barslmn ★ 2.3k
349 results • Page 1 of 7
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