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Comment: Comment: How to improve a bioinformatics study and paper so that it is not considered "to
10 weeks ago by barslmn ★ 2.3k
1
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0
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1.6k
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Comment: Comment: Good Bioinformatics Jokes/Puns?
3 months ago by barslmn ★ 2.3k
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0
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189
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Blog: Investigating male X heterozygosity in short read sequencing
heterozygosity nextflow sequencing chrX
3 months ago by barslmn ★ 2.3k
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0
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514
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Comment: Comment: Just released VEBA 2.0 in Nucleic Acids Research, a modular genome-resolved meta
3 months ago by barslmn ★ 2.3k
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0
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374
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Comment: Comment: HGNC Version Control
3 months ago by barslmn ★ 2.3k
6
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2
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374
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Tool: HGNC Version Control
git control symbols version gene
3 months ago by barslmn ★ 2.3k
1
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1
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544
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Comment: Comment: QC Analysis from Sanger sequencing
3 months ago by barslmn ★ 2.3k
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0
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456
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Comment: Comment: Odd alignment question/finding
5 months ago by barslmn ★ 2.3k
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0
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1.0k
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Comment: Comment: AGeNT LocatIt
5 months ago by barslmn ★ 2.3k
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0
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1.4k
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Comment: Comment: Why multiple SYMBOLS, Consequences... for Variant Effect Predictor (VEP)
6 months ago by barslmn ★ 2.3k
0
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1
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1.4k
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Comment: Comment: Why multiple SYMBOLS, Consequences... for Variant Effect Predictor (VEP)
6 months ago by barslmn ★ 2.3k
4
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1
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550
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Answer: Answer: Can questions and answers on biostars be asked only in English? Can't I use Russ
6 months ago by barslmn ★ 2.3k
0
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0
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1.2k
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Comment: Comment: Filtering VCF based on codon-transcript
6 months ago by barslmn ★ 2.3k
0
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1
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680
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Answer: Answer: Development plan for a bioinformatics database developer/coder
6 months ago by barslmn ★ 2.3k
0
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1
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1.2k
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Comment: Comment: Filtering VCF based on codon-transcript
6 months ago by barslmn ★ 2.3k
0
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0
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928
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Comment: Comment: I am trying to generate a bcf file through samtools mpileup but it taking too lo
6 months ago by barslmn ★ 2.3k
0
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2
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928
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Comment: Comment: I am trying to generate a bcf file through samtools mpileup but it taking too lo
6 months ago by barslmn ★ 2.3k
0
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1
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1.2k
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Comment: Comment: Filtering VCF based on codon-transcript
6 months ago by barslmn ★ 2.3k
0
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0
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333
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Comment: Comment: VEP fail to annotate NCBI refseq GFF
6 months ago by barslmn ★ 2.3k
1
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0
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455
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Comment: Comment: VCF file transfer to a better genome
6 months ago by barslmn ★ 2.3k
0
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0
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476
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Comment: Comment: Calculation variant frequencies for copy number events for a cohort
7 months ago by barslmn ★ 2.3k
2
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2
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476
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Calculation variant frequencies for copy number events for a cohort
cnv vcf variant frequency
7 months ago by barslmn ★ 2.3k
0
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1
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1.2k
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Comment: Comment: Filtering VCF based on codon-transcript
7 months ago by barslmn ★ 2.3k
1
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0
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1.5k
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Comment: Comment: Processing fastq files for genome assembly
7 months ago by barslmn ★ 2.3k
0
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1
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588
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Comment: Comment: Issues with bcftools
7 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?
7 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 7 months ago by 44k • written 7 months ago by ★ 2.3k
0
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1
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1.2k
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Comment: Comment: Filtering VCF based on codon-transcript
updated 6 months ago by 44k • written 7 months ago by ★ 2.3k
1
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0
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639
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Answer: Answer: Nextflow crash on AWS Batch with transition error
7 months ago by barslmn ★ 2.3k
1
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0
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700
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Comment: Comment: Strategies with annotated VCF files to filter very big VCF from WGS
8 months ago by barslmn ★ 2.3k
1
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0
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789
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Comment: Comment: Generate BED file
8 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
8 months ago by barslmn ★ 2.3k
1
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0
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746
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Answer: Answer: split sequences into their codons in a table
8 months ago by barslmn ★ 2.3k
1
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0
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674
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Comment: Comment: Re-format sample columns in VCF file
8 months ago by barslmn ★ 2.3k
1
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0
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829
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Comment: Comment: NF-Core
8 months ago by barslmn ★ 2.3k
0
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0
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927
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Comment: Comment: Can I remove all variants in a vcf file that have 0/0 for PRS calculation?
9 months ago by barslmn ★ 2.3k
0
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0
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1.1k
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Answer: Answer: How to rename multiple fasq files
9 months ago by barslmn ★ 2.3k
2
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0
replies
476
views
Comment: Comment: unicycler error : [Errno 13] Permission denied:
10 months ago by barslmn ★ 2.3k
0
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0
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396
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Comment: Comment: Python function to export the annotated records to genbank file using python and
10 months ago by barslmn ★ 2.3k
0
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1
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802
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Answer: Answer: AlphaMissense_hg38.tsv.gz tabix indexing issue VEP
10 months ago by barslmn ★ 2.3k
0
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0
replies
1.8k
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Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
11 months ago by barslmn ★ 2.3k
0
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1
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1.8k
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Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
11 months ago by barslmn ★ 2.3k
0
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1
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1.8k
views
Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
11 months ago by barslmn ★ 2.3k
0
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1
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1.1k
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Comment: Comment: help with weird PCA? (vcfR)
11 months ago by barslmn ★ 2.3k
0
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1
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1.8k
views
Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
11 months ago by barslmn ★ 2.3k
1
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1
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1.8k
views
Answer: Answer: Locally annotating SNP IDs and Gene names of called variants
11 months ago by barslmn ★ 2.3k
0
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1
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1.1k
views
Comment: Comment: help with weird PCA? (vcftools, Rstudio (vcfR)
11 months ago by barslmn ★ 2.3k
1
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0
replies
1.2k
views
Answer: Answer: question regarding the labeling of points on graphs generated by ggplot in R
11 months ago by barslmn ★ 2.3k
2
votes
1
reply
851
views
Comment: Comment: Calculating height prediction from PGS
11 months ago by barslmn ★ 2.3k
0
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0
replies
846
views
Comment: Comment: Confirming called variants
11 months ago by barslmn ★ 2.3k
346 results • Page 1 of 7
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