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0
votes
6
replies
2.0k
views
Getting matrix of QDs from VCF file
vcf snp
updated 3 months ago by • 0 • written 6.6 years ago by ▴ 510
2
votes
1
reply
250
views
Extract read position where a base is covered, and the allele at that base
read samtools bam mapping bwa
updated 6 months ago by 130k • written 6 months ago by ▴ 510
0
votes
1
reply
268
views
Extract mapped SE and properly paired PE reads from a bam file
properly single bam end mapped paired
updated 12 months ago by ★ 1.2k • written 12 months ago by ▴ 510
7
votes
4
replies
557
views
Alternatives to TMM normalization
voom expression R limma
15 months ago by Jautis ▴ 510
0
votes
0
replies
243
views
Using bcftools to merge files of different individuals, getting only shared sites
vcf genotypes bcftools
16 months ago by Jautis ▴ 510
2
votes
3
replies
875
views
Error running smartpca from eigensoft: failed to create thread
pca genotypes smartpca eigensoft
18 months ago by Jautis ▴ 510
2
votes
2
replies
722
views
Trim 100bp PE sequencing to 50bp reads
unix bash sequencing fastq
updated 18 months ago by 21k • written 18 months ago by ▴ 510
2
votes
2
replies
843
views
Bam file: replace low quality bases with "N"
quality base bam
20 months ago by Jautis ▴ 510
1
vote
4
replies
1.2k
views
limma+voom flips the sign of the effect from CPM?
voom expression limma R
updated 20 months ago by ★ 6.1k • written 20 months ago by ▴ 510
5
votes
5
replies
1.2k
views
voom mean-variance plot has set of genes where variance increases with expression level
voom expression limma R
updated 20 months ago by ★ 6.1k • written 20 months ago by ▴ 510
0
votes
0
replies
443
views
Calculating Fst from low coverage data using genotype likelihoods
vcftools fst population_differentiation
2.1 years ago by Jautis ▴ 510
7
votes
15
replies
6.1k
views
6 follow
Modifying fasta file based on vcf information
reference-genome vcf fasta
updated 5 months ago by 39k • written 8.0 years ago by ▴ 510
0
votes
0
replies
501
views
GO based on NCBI annotation
genome enrichment GSEA GO
2.8 years ago by Jautis ▴ 510
0
votes
0
replies
968
views
Convert VCF + LDhelmet Recombination Rates to EIGENSTRAT format
vcf linkage SNP genome
3.2 years ago by Jautis ▴ 510
0
votes
0
replies
867
views
find position of snps in cM, given recombination map from ldhelmet
recombination genome physical position
3.2 years ago by Jautis ▴ 510
2
votes
2
replies
1.6k
views
sed (or similar) command to remove part of the FORMAT from a vcf file?
vcf sed processing
updated 3.3 years ago by 16k • written 3.3 years ago by ▴ 510
1
vote
2
replies
1.5k
views
vcftools minDP filter not working for samtools genotype calling output
genotype filtering SNP SNP-calling
3.6 years ago by Jautis ▴ 510
0
votes
1
reply
774
views
Efficiently run blat for long sequences
blat alignment sequence assembly
updated 3.7 years ago by ★ 2.5k • written 3.8 years ago by ▴ 510
1
vote
1
reply
1.2k
views
Annotate CpG Islands for a new genome
CpG assembly annotation
updated 4.1 years ago by ★ 3.5k • written 4.1 years ago by ▴ 510
1
vote
8
replies
2.0k
views
Error in transferring annotations to a new assembly using RATT
alignment annotation software error Assembly
updated 4.3 years ago by 34k • written 4.4 years ago by ▴ 510
2
votes
1
reply
2.3k
views
Create a pseudo-haploid fasta file based genotype calls for an individual (vcf file)
vcf sequence assembly SNP
updated 4.6 years ago by ★ 1.6k • written 4.6 years ago by ▴ 510
0
votes
0
replies
942
views
Find SNPs which disrupt CpG sites
vcf genome variants
4.6 years ago by Jautis ▴ 510
0
votes
0
replies
1.4k
views
Determine the derived allele
alignment
4.8 years ago by Jautis ▴ 510
1
vote
2
replies
2.5k
views
GOseq with non-supported organism
GO GOseq R
4.9 years ago by Jautis ▴ 510
1
vote
5
replies
1.2k
views
Find chromosomal location of a scaffold
genome mapping
updated 4.9 years ago by 34k • written 4.9 years ago by ▴ 510
3
votes
4
replies
3.3k
views
Convert an altered sam file into a bam file
sam bam sequencing
5.5 years ago by Jautis ▴ 510
0
votes
0
replies
1.6k
views
BSMap to Bismark bam file formats
next-gen sequencing bam bisulfite
5.5 years ago by Jautis ▴ 510
0
votes
2
replies
1.1k
views
Genotype calls for a list of variable sites
genotype-calling GATK variant-calling
updated 5.6 years ago by 154k • written 5.6 years ago by ▴ 510
10
votes
4
replies
5.6k
views
Comparing two phylogenies
covariance phylogeny tree
updated 8 months ago by 39k • written 7.7 years ago by ▴ 510
2
votes
3
replies
1.6k
views
Outputting DP4 flag in GATK
variant calling sequencing gatk
updated 6.2 years ago by 5.7k • written 6.2 years ago by ▴ 510
0
votes
7
replies
1.4k
views
Getting reads that end at a digest site from a sam/bam file
bisulfite digest
updated 6.2 years ago by 154k • written 6.2 years ago by ▴ 510
0
votes
1
reply
1.7k
views
Calling allele-specific methylation from bisulfite sequencing reads
bisulfite-sequencing allele-specific sequencing
updated 6.3 years ago by 14k • written 6.4 years ago by ▴ 510
5
votes
7
replies
5.2k
views
Downsampling bam file to 2x coverage
bam sequencing high-throughput
6.4 years ago by Jautis ▴ 510
0
votes
1
reply
1.2k
views
high coverage but few genotype calls: possible causes?+
genotype calling sequencing SNP
7.0 years ago by Jautis ▴ 510
3
votes
4
replies
5.0k
views
Compare tree topologies (Newick)
tree phylogeny gene
updated 7.3 years ago by ★ 3.0k • written 7.3 years ago by ▴ 510
0
votes
1
reply
1.4k
views
Check for Msp1 digestion in sequencing data
RRBS digestion bisulfite-sequencing msp1
updated 10 months ago by 39k • written 7.4 years ago by ▴ 510
0
votes
0
replies
2.3k
views
Genome sites from BPM file
illumina location bpm
updated 10 months ago by 39k • written 7.5 years ago by ▴ 510
2
votes
2
replies
2.4k
views
Phylogenetic distance betwee species
phylogenetics newick trees
updated 10 months ago by 39k • written 7.6 years ago by ▴ 510
0
votes
2
replies
2.0k
views
Fst from 012 genotype matrix
Fst Genotype
updated 9 months ago by 39k • written 7.7 years ago by ▴ 510
2
votes
6
replies
3.2k
views
Taking genotypes out of a vcf file
vcf
updated 7 months ago by 39k • written 7.9 years ago by ▴ 510
4
votes
3
replies
2.0k
views
Making a haploid genome
vcf haploid-genome variant
updated 6 months ago by 39k • written 7.9 years ago by ▴ 510
0
votes
1
reply
2.4k
views
Masking Variable Sites in a Fasta File
fasta vcf
updated 5 months ago by 39k • written 8.0 years ago by ▴ 510
0
votes
1
reply
2.8k
views
Finding differences between 2 fasta files
fasta
updated 5 months ago by 39k • written 8.0 years ago by ▴ 510
6
votes
4
replies
2.3k
views
Help simulating RRBS reads
methylation RRBS
updated 4 months ago by 39k • written 8.0 years ago by ▴ 510
7
votes
5
replies
2.2k
views
Filter fastq file by first two base pairs
fastq
updated 4 months ago by 39k • written 8.1 years ago by ▴ 510
6
votes
2
replies
1.4k
views
Comparing methods to genotype
RNA-Seq genotyping vcf RRBS
updated 11 months ago by 39k • written 8.1 years ago by ▴ 510
1
vote
6
replies
3.0k
views
Calling SNPs from RRBS data
SNP RRBS SNP-calling bisulfite-sequencing
updated 13 months ago by 39k • written 8.3 years ago by ▴ 510
47 results • Page 1 of 1
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