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Comment: C: why different outputs with applying various extracting fasta sequences tool, whi
updated 5.5 years ago by 45k • written 9.8 years ago by ★ 1.9k
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1
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5.7k
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Comment: C: Fasta sequence replacement based on header name
updated 5.5 years ago by 45k • written 9.9 years ago by ★ 1.9k
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1
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5.7k
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Comment: C: Fasta sequence replacement based on header name
updated 5.5 years ago by 45k • written 9.9 years ago by ★ 1.9k
0
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1
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5.7k
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Comment: C: Fasta sequence replacement based on header name
updated 5.5 years ago by 45k • written 9.9 years ago by ★ 1.9k
1
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2
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12k
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Comment: C: FASTA sequence extraction using list of sequence name that are not identical wit
updated 5.6 years ago by 45k • written 9.9 years ago by ★ 1.9k
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6.2k
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Comment: C: exact command for read normalization using trinity software
updated 5.6 years ago by 45k • written 10.5 years ago by ★ 1.9k
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3.9k
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Comment: C: how to set CPU with butterfly dependency RAM (bflyHeapSpaceMax) in trinity assem
updated 5.6 years ago by 45k • written 10.5 years ago by ★ 1.9k
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1
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1.6k
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Comment: C: Gene-based common and rare variant association analysis
5.7 years ago by seta ★ 1.9k
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3.0k
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Comment: C: Getting a sample of 1000 random SNPs with MAF
5.8 years ago by seta ★ 1.9k
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1.3k
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Comment: C: bedtools closest return no output!
5.9 years ago by seta ★ 1.9k
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1
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1.5k
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Comment: C: Convert HLA allele to Genepop format
5.9 years ago by seta ★ 1.9k
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1
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1.5k
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Comment: C: Convert HLA allele to Genepop format
5.9 years ago by seta ★ 1.9k
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1.1k
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Comment: C: Recoding HLA Alleles by 01
5.9 years ago by seta ★ 1.9k
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3.1k
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Comment: C: Calculating Fst from simulations
5.9 years ago by seta ★ 1.9k
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10k
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Comment: C: Picking random SNPs from 1000 Genomes using Vcftools
5.9 years ago by seta ★ 1.9k
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14k
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Comment: C: Unexpected outcome: Gene Enrichment using Fisher's Test
5.9 years ago by seta ★ 1.9k
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1.5k
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Comment: C: Selection of random SNPs with similar allele frequency with my SNPs under study
5.9 years ago by seta ★ 1.9k
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0
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10k
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Comment: C: Picking random SNPs from 1000 Genomes using Vcftools
5.9 years ago by seta ★ 1.9k
0
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1
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29k
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Comment: C: Ibd (Identity By Descent) And The Chosen Value Of Pi_Hat
5.9 years ago by seta ★ 1.9k
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2
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8.7k
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Comment: C: Removing homozygous reference genotypes from multi-sample vcf file
5.9 years ago by seta ★ 1.9k
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1
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8.7k
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Comment: C: Removing homozygous reference genotypes from vcf file
5.9 years ago by seta ★ 1.9k
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2.1k
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Comment: C: Insert size distribution for BWA
5.9 years ago by seta ★ 1.9k
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11k
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Comment: C: Skip orientation as there are not enough pairs by bwa mem
5.9 years ago by seta ★ 1.9k
0
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1
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11k
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Comment: C: Skip orientation as there are not enough pairs by bwa mem
5.9 years ago by seta ★ 1.9k
0
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1
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11k
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Comment: C: Skip orientation as there are not enough pairs by bwa mem
5.9 years ago by seta ★ 1.9k
0
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1
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2.1k
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Comment: C: Insert size distribution for BWA
5.9 years ago by seta ★ 1.9k
0
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2
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2.1k
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Comment: C: Insert size distribution for BWA
5.9 years ago by seta ★ 1.9k
0
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0
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11k
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Comment: C: Realign BAM files to other reference file
6.0 years ago by seta ★ 1.9k
0
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1
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11k
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Comment: C: Realign BAM files to other reference file
6.0 years ago by seta ★ 1.9k
0
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2
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11k
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Comment: C: Skip orientation as there are not enough pairs by bwa mem
6.0 years ago by seta ★ 1.9k
0
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1
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11k
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Comment: C: Skip orientation as there are not enough pairs by bwa mem
updated 6.0 years ago by 35k • written 6.0 years ago by ★ 1.9k
0
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1
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11k
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Comment: C: Skip orientation as there are not enough pairs by bwa mem
6.0 years ago by seta ★ 1.9k
0
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2
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11k
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Comment: C: Skip orientation as there are not enough pairs by bwa mem
6.0 years ago by seta ★ 1.9k
0
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0
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11k
views
Comment: C: Skip orientation as there are not enough pairs by bwa mem
6.0 years ago by seta ★ 1.9k
0
votes
1
reply
11k
views
Comment: C: Skip orientation as there are not enough pairs by bwa mem
6.0 years ago by seta ★ 1.9k
0
votes
1
reply
11k
views
Comment: C: Realign BAM files to other reference file
6.0 years ago by seta ★ 1.9k
0
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0
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1.9k
views
Comment: C: BWA alignment and very low properly paired
6.0 years ago by seta ★ 1.9k
0
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0
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3.0k
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Comment: C: Keeping only common variants in the merged VCF file
6.0 years ago by seta ★ 1.9k
0
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0
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1.6k
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Comment: C: Getting Ensembl gene ID via biomart
6.0 years ago by seta ★ 1.9k
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0
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1.6k
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Comment: C: Getting Ensembl gene ID via biomart
6.0 years ago by seta ★ 1.9k
0
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0
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4.4k
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Comment: C: HLA allele visualization in BAM file
6.0 years ago by seta ★ 1.9k
0
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1
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4.4k
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Comment: C: HLA allele visualization in BAM file
6.0 years ago by seta ★ 1.9k
0
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1
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4.4k
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Comment: C: HLA allele visualization in BAM file
6.0 years ago by seta ★ 1.9k
0
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1
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4.4k
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Comment: C: HLA allele visualization in BAM file
6.0 years ago by seta ★ 1.9k
0
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1
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4.4k
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Comment: C: HLA allele visualization in BAM file
6.0 years ago by seta ★ 1.9k
0
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1
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1.5k
views
Comment: C: The content of variation (VEP) file from Ensembl
6.1 years ago by seta ★ 1.9k
0
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1
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1.5k
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Comment: C: The content of variation (VEP) file from Ensembl
6.1 years ago by seta ★ 1.9k
0
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0
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8.7k
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Comment: A: why A/T or C/G are ambiguous SNPs?
6.1 years ago by seta ★ 1.9k
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1
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4.2k
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Comment: C: How to check the allele strand of variants?
6.1 years ago by seta ★ 1.9k
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1
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2.4k
views
Comment: C: DE analysis with edgeR and possibly batch effect
6.2 years ago by seta ★ 1.9k
542 results • Page 4 of 11
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