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Comment: Comment: Odd alignment question/finding
15 days ago by barslmn ★ 2.2k
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866
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Comment: Comment: AGeNT LocatIt
24 days ago by barslmn ★ 2.2k
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1.1k
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Comment: Comment: Why multiple SYMBOLS, Consequences... for Variant Effect Predictor (VEP)
7 weeks ago by barslmn ★ 2.2k
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1
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1.1k
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Comment: Comment: Why multiple SYMBOLS, Consequences... for Variant Effect Predictor (VEP)
7 weeks ago by barslmn ★ 2.2k
3
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1
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409
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Answer: Answer: Can questions and answers on biostars be asked only in English? Can't I use Russ
7 weeks ago by barslmn ★ 2.2k
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0
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850
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Comment: Comment: Filtering VCF based on codon-transcript
9 weeks ago by barslmn ★ 2.2k
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1
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514
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Answer: Answer: Development plan for a bioinformatics database developer/coder
9 weeks ago by barslmn ★ 2.2k
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1
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850
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Comment: Comment: Filtering VCF based on codon-transcript
9 weeks ago by barslmn ★ 2.2k
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0
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702
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Comment: Comment: I am trying to generate a bcf file through samtools mpileup but it taking too lo
9 weeks ago by barslmn ★ 2.2k
0
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2
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702
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Comment: Comment: I am trying to generate a bcf file through samtools mpileup but it taking too lo
9 weeks ago by barslmn ★ 2.2k
0
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1
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850
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Comment: Comment: Filtering VCF based on codon-transcript
9 weeks ago by barslmn ★ 2.2k
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225
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Comment: Comment: VEP fail to annotate NCBI refseq GFF
9 weeks ago by barslmn ★ 2.2k
1
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0
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355
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Comment: Comment: VCF file transfer to a better genome
9 weeks ago by barslmn ★ 2.2k
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0
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335
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Comment: Comment: Calculation variant frequencies for copy number events for a cohort
10 weeks ago by barslmn ★ 2.2k
2
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2
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335
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Calculation variant frequencies for copy number events for a cohort
cnv vcf variant frequency
10 weeks ago by barslmn ★ 2.2k
0
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1
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850
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Comment: Comment: Filtering VCF based on codon-transcript
10 weeks ago by barslmn ★ 2.2k
1
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0
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998
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Comment: Comment: Processing fastq files for genome assembly
10 weeks ago by barslmn ★ 2.2k
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1
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448
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Comment: Comment: Issues with bcftools
10 weeks ago by barslmn ★ 2.2k
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0
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16k
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Comment: Comment: Issues installing bcl2fastq?
10 weeks ago by barslmn ★ 2.2k
1
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0
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16k
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Comment: Comment: Issues installing bcl2fastq?
updated 10 weeks ago by 43k • written 10 weeks ago by ★ 2.2k
0
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1
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850
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Comment: Comment: Filtering VCF based on codon-transcript
updated 9 weeks ago by 43k • written 10 weeks ago by ★ 2.2k
1
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0
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372
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Answer: Answer: Nextflow crash on AWS Batch with transition error
10 weeks ago by barslmn ★ 2.2k
1
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0
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496
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Comment: Comment: Strategies with annotated VCF files to filter very big VCF from WGS
3 months ago by barslmn ★ 2.2k
1
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0
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603
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Comment: Comment: Generate BED file
3 months ago by barslmn ★ 2.2k
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0
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1.4k
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Comment: Comment: Error message: "separator must begin with the '+' sign. cluster 1" during Fastq
3 months ago by barslmn ★ 2.2k
1
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0
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598
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Answer: Answer: split sequences into their codons in a table
4 months ago by barslmn ★ 2.2k
1
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0
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528
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Comment: Comment: Re-format sample columns in VCF file
4 months ago by barslmn ★ 2.2k
1
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0
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602
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Comment: Comment: NF-Core
4 months ago by barslmn ★ 2.2k
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0
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762
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Comment: Comment: Can I remove all variants in a vcf file that have 0/0 for PRS calculation?
4 months ago by barslmn ★ 2.2k
0
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0
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912
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Answer: Answer: How to rename multiple fasq files
4 months ago by barslmn ★ 2.2k
2
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0
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348
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Comment: Comment: unicycler error : [Errno 13] Permission denied:
5 months ago by barslmn ★ 2.2k
0
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0
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293
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Comment: Comment: Python function to export the annotated records to genbank file using python and
5 months ago by barslmn ★ 2.2k
0
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1
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547
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Answer: Answer: AlphaMissense_hg38.tsv.gz tabix indexing issue VEP
6 months ago by barslmn ★ 2.2k
0
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0
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1.4k
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Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
6 months ago by barslmn ★ 2.2k
0
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1
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1.4k
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Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
6 months ago by barslmn ★ 2.2k
0
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1
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1.4k
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Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
6 months ago by barslmn ★ 2.2k
0
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1
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924
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Comment: Comment: help with weird PCA? (vcfR)
6 months ago by barslmn ★ 2.2k
0
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1
reply
1.4k
views
Comment: Comment: Locally annotating SNP IDs and Gene names of called variants
6 months ago by barslmn ★ 2.2k
1
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1
reply
1.4k
views
Answer: Answer: Locally annotating SNP IDs and Gene names of called variants
6 months ago by barslmn ★ 2.2k
0
votes
1
reply
924
views
Comment: Comment: help with weird PCA? (vcftools, Rstudio (vcfR)
6 months ago by barslmn ★ 2.2k
1
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0
replies
965
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Answer: Answer: question regarding the labeling of points on graphs generated by ggplot in R
6 months ago by barslmn ★ 2.2k
2
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1
reply
684
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Comment: Comment: Calculating height prediction from PGS
6 months ago by barslmn ★ 2.2k
0
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0
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697
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Comment: Comment: Confirming called variants
6 months ago by barslmn ★ 2.2k
0
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1
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804
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Comment: Comment: how can i solve a problem in applying a mutation on protein sequence?
6 months ago by barslmn ★ 2.2k
0
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1
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697
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Comment: Comment: Confirming called variants
6 months ago by barslmn ★ 2.2k
0
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0
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1.2k
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Comment: Comment: NGS one-liner to call variants
6 months ago by barslmn ★ 2.2k
1
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1
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1.2k
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Comment: Comment: NGS one-liner to call variants
6 months ago by barslmn ★ 2.2k
0
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1
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1.2k
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Comment: Comment: NGS one-liner to call variants
6 months ago by barslmn ★ 2.2k
0
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0
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1.4k
views
Comment: Comment: VEP ensemble docker and plugins
6 months ago by barslmn ★ 2.2k
0
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0
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1.2k
views
Comment: Comment: NGS one-liner to call variants
6 months ago by barslmn ★ 2.2k
339 results • Page 1 of 7
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