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748
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Comment: Comment: Variant effect predictor in ictalurus punctatus
22 months ago by barslmn ★ 2.3k
2
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1
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892
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Answer: Answer: Annotating snps with gene information
22 months ago by barslmn ★ 2.3k
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0
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2.7k
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Comment: Comment: Sequence Alignment from Scratch with BWA
22 months ago by barslmn ★ 2.3k
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1
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1.4k
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Comment: Comment: Bioconductor drawProteins alternative in Python
22 months ago by barslmn ★ 2.3k
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0
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948
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Comment: Comment: How can I construct the adjacency matrix for gene ontology between genes
22 months ago by barslmn ★ 2.3k
1
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1
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948
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Answer: Answer: How can I construct the adjacency matrix for gene ontology between genes
22 months ago by barslmn ★ 2.3k
1
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1
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1.2k
views
Comment: Comment: Bedtools give different output
22 months ago by barslmn ★ 2.3k
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1
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1.2k
views
Comment: Comment: Bedtools give different output
22 months ago by barslmn ★ 2.3k
1
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1
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1.2k
views
Answer: Answer: Bedtools give different output
22 months ago by barslmn ★ 2.3k
0
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1
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769
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Comment: Comment: Reomve the first occurance of overalapping variants from VCF file
22 months ago by barslmn ★ 2.3k
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0
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942
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Answer: Answer: GO ontology
22 months ago by barslmn ★ 2.3k
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1
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2.0k
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Comment: Comment: Comparing the GVF file & VCF file
22 months ago by barslmn ★ 2.3k
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0
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2.1k
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Comment: Comment: convert tsv file to VCF
22 months ago by barslmn ★ 2.3k
0
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1
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907
views
Comment: Comment: How to extract sequence in fasta format from micro RNA gff3 files (sRNAanno data
22 months ago by barslmn ★ 2.3k
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1
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732
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Comment: Comment: script for local blast to mapped primer to the genome
22 months ago by barslmn ★ 2.3k
2
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0
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1.1k
views
Comment: Comment: Creating Gene ID and Gene name colum from FASTA IDs
22 months ago by barslmn ★ 2.3k
1
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1
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1.1k
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Comment: Comment: Creating Gene ID and Gene name colum from FASTA IDs
22 months ago by barslmn ★ 2.3k
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0
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947
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Comment: Comment: CNV calling
22 months ago by barslmn ★ 2.3k
12
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7
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2.7k
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Tutorial: Sequence Alignment from Scratch with BWA
alignment bwa DNA
20 months ago by barslmn ★ 2.3k
0
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0
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1.0k
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Comment: Comment: Removing individuals and plotting Allele Frequency Difference plots from a vcf f
22 months ago by barslmn ★ 2.3k
1
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1
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1.0k
views
Comment: Comment: Removing individuals and plotting Allele Frequency Difference plots from a vcf f
22 months ago by barslmn ★ 2.3k
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0
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887
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Comment: Comment: Mutation data with Variant Allele Frequency at CbioPortal
22 months ago by barslmn ★ 2.3k
2
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1
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768
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Answer: Answer: Looking for list(s) of human genes which are differentially expressed between ma
22 months ago by barslmn ★ 2.3k
0
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0
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588
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Comment: Comment: Filter VEP for same entry
22 months ago by barslmn ★ 2.3k
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1
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2.0k
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Comment: Comment: Stringtie issue. "Error: no valid ID found for GFF record"
22 months ago by barslmn ★ 2.3k
1
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1
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2.0k
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Comment: Comment: Stringtie issue. "Error: no valid ID found for GFF record"
22 months ago by barslmn ★ 2.3k
3
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1
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3.4k
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Tutorial: Converting TSV file to VCF
vcf preprocessing frequency
updated 22 months ago by 164k • written 22 months ago by ★ 2.3k
1
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0
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1.2k
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Comment: Comment: Predicting protein fold using known stracture
22 months ago by barslmn ★ 2.3k
1
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1
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2.0k
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Comment: Comment: Error after installation of AGAT
22 months ago by barslmn ★ 2.3k
0
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1
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2.0k
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Comment: Comment: Error after installation of AGAT
22 months ago by barslmn ★ 2.3k
0
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0
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1.3k
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Comment: Comment: I want to merge gene sequences in fasta to create one genome from all cds region
22 months ago by barslmn ★ 2.3k
0
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0
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2.0k
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Comment: Comment: Error after installation of AGAT
22 months ago by barslmn ★ 2.3k
1
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1
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832
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Comment: Comment: Scaling to remove Whitespace not working in ClusterProfiler
22 months ago by barslmn ★ 2.3k
0
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1
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688
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Answer: Answer: Visualization of Pedigree reconstruction
22 months ago by barslmn ★ 2.3k
1
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1
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3.5k
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Comment: Comment: Randomly select a number of variants and samples from a multi-sample VCF file (p
22 months ago by barslmn ★ 2.3k
0
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0
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1.1k
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Comment: Comment: gene ontology of a certain gene names
22 months ago by barslmn ★ 2.3k
0
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0
replies
1.5k
views
Comment: Comment: Retrieve count table from bam file using genomic coordinates
22 months ago by barslmn ★ 2.3k
0
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1
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1.5k
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Comment: Comment: Retrieve count table from bam file using genomic coordinates
22 months ago by barslmn ★ 2.3k
0
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0
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1.2k
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Comment: Comment: VCF file evaluation
22 months ago by barslmn ★ 2.3k
0
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0
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1.6k
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Comment: Comment: Does a merged VCF file (using bcftools merge) contain unique SNPs or INDELs fro
22 months ago by barslmn ★ 2.3k
0
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1
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1.9k
views
Comment: Comment: how to create a distance matrix from huge file of nucleotide sequence using R- l
22 months ago by barslmn ★ 2.3k
1
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1
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3.6k
views
Comment: Comment: error in pipeline installation dependent on numpy version 1.18.5
22 months ago by barslmn ★ 2.3k
1
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0
replies
1.5k
views
Comment: Comment: bowtie2, and python script
22 months ago by barslmn ★ 2.3k
0
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0
replies
1.6k
views
Answer: Answer: Does a merged VCF file (using bcftools merge) contain unique SNPs or INDELs fro
22 months ago by barslmn ★ 2.3k
0
votes
1
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846
views
Comment: Comment: Spatial spots deconvolution
22 months ago by barslmn ★ 2.3k
1
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0
replies
1.2k
views
Comment: Comment: R packages
22 months ago by barslmn ★ 2.3k
3
votes
1
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787
views
Answer: Answer: limiting functions to some columns in r
22 months ago by barslmn ★ 2.3k
2
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1
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1000
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Comment: Comment: Gene coverage plots from a data frame on tiling amplicon sequencing data
22 months ago by barslmn ★ 2.3k
3
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1
reply
1.5k
views
Answer: Answer: bowtie2, and python script
22 months ago by barslmn ★ 2.3k
1
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1
reply
1.1k
views
Comment: Comment: gene ontology of a certain gene names
22 months ago by barslmn ★ 2.3k
349 results • Page 4 of 7
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