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Comment: Comment: Why multiple SYMBOLS, Consequences... for Variant Effect Predictor (VEP)
22 days ago by barslmn ★ 2.1k
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1.0k
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Comment: Comment: Why multiple SYMBOLS, Consequences... for Variant Effect Predictor (VEP)
23 days ago by barslmn ★ 2.1k
3
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368
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Answer: Answer: Can questions and answers on biostars be asked only in English? Can't I use Russ
23 days ago by barslmn ★ 2.1k
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766
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Comment: Comment: Filtering VCF based on codon-transcript
4 weeks ago by barslmn ★ 2.1k
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460
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Answer: Answer: Development plan for a bioinformatics database developer/coder
4 weeks ago by barslmn ★ 2.1k
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766
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Comment: Comment: Filtering VCF based on codon-transcript
5 weeks ago by barslmn ★ 2.1k
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0
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656
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Comment: Comment: I am trying to generate a bcf file through samtools mpileup but it taking too lo
5 weeks ago by barslmn ★ 2.1k
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2
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656
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Comment: Comment: I am trying to generate a bcf file through samtools mpileup but it taking too lo
5 weeks ago by barslmn ★ 2.1k
0
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1
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766
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Comment: Comment: Filtering VCF based on codon-transcript
5 weeks ago by barslmn ★ 2.1k
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179
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Comment: Comment: VEP fail to annotate NCBI refseq GFF
5 weeks ago by barslmn ★ 2.1k
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319
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Comment: Comment: VCF file transfer to a better genome
5 weeks ago by barslmn ★ 2.1k
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291
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Comment: Comment: Calculation variant frequencies for copy number events for a cohort
5 weeks ago by barslmn ★ 2.1k
2
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2
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291
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Calculation variant frequencies for copy number events for a cohort
cnv vcf variant frequency
5 weeks ago by barslmn ★ 2.1k
0
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1
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766
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Comment: Comment: Filtering VCF based on codon-transcript
5 weeks ago by barslmn ★ 2.1k
1
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0
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857
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Comment: Comment: Processing fastq files for genome assembly
5 weeks ago by barslmn ★ 2.1k
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1
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398
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Comment: Comment: Issues with bcftools
5 weeks ago by barslmn ★ 2.1k
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16k
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Comment: Comment: Issues installing bcl2fastq?
6 weeks ago by barslmn ★ 2.1k
1
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16k
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Comment: Comment: Issues installing bcl2fastq?
updated 6 weeks ago by 43k • written 6 weeks ago by ★ 2.1k
0
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1
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766
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Comment: Comment: Filtering VCF based on codon-transcript
updated 4 weeks ago by 43k • written 6 weeks ago by ★ 2.1k
1
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303
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Answer: Answer: Nextflow crash on AWS Batch with transition error
6 weeks ago by barslmn ★ 2.1k
1
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0
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418
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Comment: Comment: Strategies with annotated VCF files to filter very big VCF from WGS
10 weeks ago by barslmn ★ 2.1k
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0
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543
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Comment: Comment: Generate BED file
10 weeks ago by barslmn ★ 2.1k
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1.3k
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Comment: Comment: Error message: "separator must begin with the '+' sign. cluster 1" during Fastq
11 weeks ago by barslmn ★ 2.1k
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550
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Answer: Answer: split sequences into their codons in a table
12 weeks ago by barslmn ★ 2.1k
1
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0
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473
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Comment: Comment: Re-format sample columns in VCF file
12 weeks ago by barslmn ★ 2.1k
1
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0
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550
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Comment: Comment: NF-Core
3 months ago by barslmn ★ 2.1k
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0
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686
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Comment: Comment: Can I remove all variants in a vcf file that have 0/0 for PRS calculation?
3 months ago by barslmn ★ 2.1k
0
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0
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842
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Answer: Answer: How to rename multiple fasq files
3 months ago by barslmn ★ 2.1k
2
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0
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321
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Comment: Comment: unicycler error : [Errno 13] Permission denied:
4 months ago by barslmn ★ 2.1k
0
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0
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277
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Comment: Comment: Python function to export the annotated records to genbank file using python and
4 months ago by barslmn ★ 2.1k
0
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1
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472
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Answer: Answer: AlphaMissense_hg38.tsv.gz tabix indexing issue VEP
5 months ago by barslmn ★ 2.1k
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0
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1.3k
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Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
5 months ago by barslmn ★ 2.1k
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1
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1.3k
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Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
5 months ago by barslmn ★ 2.1k
0
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1
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1.3k
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Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
5 months ago by barslmn ★ 2.1k
0
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1
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859
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Comment: Comment: help with weird PCA? (vcfR)
5 months ago by barslmn ★ 2.1k
0
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1
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1.3k
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Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
5 months ago by barslmn ★ 2.1k
1
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1
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1.3k
views
Answer: Answer: Locally annotating SNP IDs and Gene names of called variants
5 months ago by barslmn ★ 2.1k
0
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1
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859
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Comment: Comment: help with weird PCA? (vcftools, Rstudio (vcfR)
5 months ago by barslmn ★ 2.1k
1
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0
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896
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Answer: Answer: question regarding the labeling of points on graphs generated by ggplot in R
5 months ago by barslmn ★ 2.1k
2
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1
reply
639
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Comment: Comment: Calculating height prediction from PGS
5 months ago by barslmn ★ 2.1k
0
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0
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638
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Comment: Comment: Confirming called variants
5 months ago by barslmn ★ 2.1k
0
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1
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741
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Comment: Comment: how can i solve a problem in applying a mutation on protein sequence?
5 months ago by barslmn ★ 2.1k
0
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1
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638
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Comment: Comment: Confirming called variants
5 months ago by barslmn ★ 2.1k
0
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0
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1.1k
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Comment: Comment: NGS one-liner to call variants
5 months ago by barslmn ★ 2.1k
1
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1
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1.1k
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Comment: Comment: NGS one-liner to call variants
5 months ago by barslmn ★ 2.1k
0
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1
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1.1k
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Comment: Comment: NGS one-liner to call variants
5 months ago by barslmn ★ 2.1k
0
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0
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1.3k
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Comment: Comment: VEP ensemble docker and plugins
5 months ago by barslmn ★ 2.1k
0
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0
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1.1k
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Comment: Comment: NGS one-liner to call variants
5 months ago by barslmn ★ 2.1k
0
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0
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334
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Comment: Comment: Pysam pileup and Rsamtools pileup output discrepancy
5 months ago by barslmn ★ 2.1k
16
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9
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1.1k
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Blog: NGS one-liner to call variants
shell sequencing
updated 5 months ago by 43k • written 5 months ago by ★ 2.1k
337 results • Page 1 of 7
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