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Answer: Answer: Pipeline for Illumina GSAv3 in Beagle, ADMIXTURE and qpAdm?
3 months ago by barslmn ★ 2.3k
2
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747
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Answer: Answer: STAR alignment for RNA seq - trouble occurred
3 months ago by barslmn ★ 2.3k
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0
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572
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Comment: Comment: A notebook for checking relatedness and X heterozygosity from sequencing data
4 months ago by barslmn ★ 2.3k
4
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2
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572
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Tool: A notebook for checking relatedness and X heterozygosity from sequencing data
heterozygosity relatedness sequencing sex estimation
4 months ago by barslmn ★ 2.3k
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0
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419
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Answer: Answer: Minor Allele Frequency Calculation for 23andMe data
4 months ago by barslmn ★ 2.3k
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1
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2.0k
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Comment: Comment: How to improve a bioinformatics study and paper so that it is not considered "to
7 months ago by barslmn ★ 2.3k
1
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0
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2.9k
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Comment: Comment: Good Bioinformatics Jokes/Puns?
8 months ago by barslmn ★ 2.3k
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0
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303
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Blog: Investigating male X heterozygosity in short read sequencing
heterozygosity nextflow sequencing chrX
8 months ago by barslmn ★ 2.3k
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0
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1.2k
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Comment: Comment: Just released VEBA 2.0 in Nucleic Acids Research, a modular genome-resolved meta
8 months ago by barslmn ★ 2.3k
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0
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565
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Comment: Comment: HGNC Version Control
8 months ago by barslmn ★ 2.3k
6
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2
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565
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Tool: HGNC Version Control
git control symbols version gene
8 months ago by barslmn ★ 2.3k
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1
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851
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Comment: Comment: QC Analysis from Sanger sequencing
9 months ago by barslmn ★ 2.3k
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631
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Comment: Comment: Odd alignment question/finding
10 months ago by barslmn ★ 2.3k
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0
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1.2k
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Comment: Comment: AGeNT LocatIt
10 months ago by barslmn ★ 2.3k
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0
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1.9k
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Comment: Comment: Why multiple SYMBOLS, Consequences... for Variant Effect Predictor (VEP)
11 months ago by barslmn ★ 2.3k
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1
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1.9k
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Comment: Comment: Why multiple SYMBOLS, Consequences... for Variant Effect Predictor (VEP)
11 months ago by barslmn ★ 2.3k
4
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1
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743
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Answer: Answer: Can questions and answers on biostars be asked only in English? Can't I use Russ
11 months ago by barslmn ★ 2.3k
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0
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1.7k
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Comment: Comment: Filtering VCF based on codon-transcript
12 months ago by barslmn ★ 2.3k
0
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1
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907
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Answer: Answer: Development plan for a bioinformatics database developer/coder
12 months ago by barslmn ★ 2.3k
0
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1
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1.7k
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Comment: Comment: Filtering VCF based on codon-transcript
12 months ago by barslmn ★ 2.3k
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0
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1.2k
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Comment: Comment: I am trying to generate a bcf file through samtools mpileup but it taking too lo
12 months ago by barslmn ★ 2.3k
0
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2
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1.2k
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Comment: Comment: I am trying to generate a bcf file through samtools mpileup but it taking too lo
12 months ago by barslmn ★ 2.3k
0
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1
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1.7k
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Comment: Comment: Filtering VCF based on codon-transcript
12 months ago by barslmn ★ 2.3k
0
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0
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478
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Comment: Comment: VEP fail to annotate NCBI refseq GFF
12 months ago by barslmn ★ 2.3k
1
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0
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632
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Comment: Comment: VCF file transfer to a better genome
12 months ago by barslmn ★ 2.3k
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0
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680
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Comment: Comment: Calculation variant frequencies for copy number events for a cohort
12 months ago by barslmn ★ 2.3k
2
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2
replies
680
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Calculation variant frequencies for copy number events for a cohort
cnv vcf variant frequency
12 months ago by barslmn ★ 2.3k
0
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1
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1.7k
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Comment: Comment: Filtering VCF based on codon-transcript
12 months ago by barslmn ★ 2.3k
1
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0
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2.0k
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Comment: Comment: Processing fastq files for genome assembly
12 months ago by barslmn ★ 2.3k
0
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1
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780
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Comment: Comment: Issues with bcftools
12 months ago by barslmn ★ 2.3k
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0
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19k
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Comment: Comment: Issues installing bcl2fastq?
12 months ago by barslmn ★ 2.3k
1
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0
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19k
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Comment: Comment: Issues installing bcl2fastq?
updated 12 months ago by 45k • written 12 months ago by ★ 2.3k
0
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1
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1.7k
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Comment: Comment: Filtering VCF based on codon-transcript
updated 12 months ago by 45k • written 12 months ago by ★ 2.3k
1
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0
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978
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Answer: Answer: Nextflow crash on AWS Batch with transition error
12 months ago by barslmn ★ 2.3k
1
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0
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901
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Comment: Comment: Strategies with annotated VCF files to filter very big VCF from WGS
13 months ago by barslmn ★ 2.3k
1
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0
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1.0k
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Comment: Comment: Generate BED file
13 months ago by barslmn ★ 2.3k
0
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0
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1.8k
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Comment: Comment: Error message: "separator must begin with the '+' sign. cluster 1" during Fastq
13 months ago by barslmn ★ 2.3k
1
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0
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959
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Answer: Answer: split sequences into their codons in a table
14 months ago by barslmn ★ 2.3k
1
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0
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863
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Comment: Comment: Re-format sample columns in VCF file
14 months ago by barslmn ★ 2.3k
1
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0
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1.1k
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Comment: Comment: NF-Core
14 months ago by barslmn ★ 2.3k
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0
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1.2k
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Comment: Comment: Can I remove all variants in a vcf file that have 0/0 for PRS calculation?
14 months ago by barslmn ★ 2.3k
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0
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1.5k
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Answer: Answer: How to rename multiple fasq files
14 months ago by barslmn ★ 2.3k
2
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0
replies
653
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Comment: Comment: unicycler error : [Errno 13] Permission denied:
15 months ago by barslmn ★ 2.3k
0
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0
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516
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Comment: Comment: Python function to export the annotated records to genbank file using python and
15 months ago by barslmn ★ 2.3k
0
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1
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1.2k
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Answer: Answer: AlphaMissense_hg38.tsv.gz tabix indexing issue VEP
16 months ago by barslmn ★ 2.3k
0
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0
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2.5k
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Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
16 months ago by barslmn ★ 2.3k
0
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1
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2.5k
views
Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
16 months ago by barslmn ★ 2.3k
0
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1
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2.5k
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Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
16 months ago by barslmn ★ 2.3k
0
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1
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1.4k
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Comment: Comment: help with weird PCA? (vcfR)
16 months ago by barslmn ★ 2.3k
0
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1
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2.5k
views
Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
16 months ago by barslmn ★ 2.3k
351 results • Page 1 of 8
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