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Showing :
questions
4
votes
1
reply
457
views
LD-prune variants while maintaining a list of SNPs
snp
vcf
plink
filtering
independent
updated 7 months ago by
zx8754
12k • written 7 months ago by
Jautis
▴ 580
0
votes
0
replies
379
views
Troubleshooting error with BSmooth: `error in serialize(data, node$con)`
R
sequencing
methylation
bsseq
updated 5 months ago by
Ram
44k • written 10 months ago by
Jautis
▴ 580
1
vote
1
reply
416
views
Match variants for allele frequency, LD score, and other features
snp
12 months ago by
Jautis
▴ 580
0
votes
6
replies
2.7k
views
Getting matrix of QDs from VCF file
vcf
snp
updated 21 months ago by
wlei091226
• 0 • written 8.1 years ago by
Jautis
▴ 580
2
votes
1
reply
485
views
Extract read position where a base is covered, and the allele at that base
samtools
bam
bwa
updated 17 months ago by
Ram
44k • written 2.1 years ago by
Jautis
▴ 580
0
votes
1
reply
550
views
Extract mapped SE and properly paired PE reads from a bam file
properly
single
bam
end
mapped
paired
updated 2.5 years ago by
jv
★ 1.8k • written 2.5 years ago by
Jautis
▴ 580
7
votes
4
replies
1.1k
views
Alternatives to TMM normalization
voom
expression
R
limma
2.7 years ago by
Jautis
▴ 580
0
votes
0
replies
448
views
Using bcftools to merge files of different individuals, getting only shared sites
vcf
genotypes
bcftools
2.9 years ago by
Jautis
▴ 580
2
votes
3
replies
1.5k
views
Error running smartpca from eigensoft: failed to create thread
pca
genotypes
smartpca
eigensoft
3.0 years ago by
Jautis
▴ 580
2
votes
2
replies
1.3k
views
Trim 100bp PE sequencing to 50bp reads
unix
bash
sequencing
fastq
updated 3.0 years ago by
cpad0112
21k • written 3.0 years ago by
Jautis
▴ 580
2
votes
2
replies
1.4k
views
Bam file: replace low quality bases with "N"
quality
base
bam
3.1 years ago by
Jautis
▴ 580
1
vote
4
replies
1.9k
views
limma+voom flips the sign of the effect from CPM?
voom
expression
limma
R
updated 3.2 years ago by
Gordon Smyth
★ 7.7k • written 3.2 years ago by
Jautis
▴ 580
6
votes
5
replies
2.1k
views
voom mean-variance plot has set of genes where variance increases with expression level
voom
expression
limma
R
updated 3.2 years ago by
Gordon Smyth
★ 7.7k • written 3.2 years ago by
Jautis
▴ 580
1
vote
0
replies
681
views
Calculating Fst from low coverage data using genotype likelihoods
vcftools
fst
population_differentiation
3.6 years ago by
Jautis
▴ 580
7
votes
15
replies
7.5k
views
6 follow
Modifying fasta file based on vcf information
reference-genome
vcf
fasta
updated 23 months ago by
Ram
44k • written 9.5 years ago by
Jautis
▴ 580
0
votes
0
replies
672
views
GO based on NCBI annotation
genome
enrichment
GSEA
GO
4.3 years ago by
Jautis
▴ 580
0
votes
0
replies
1.2k
views
Convert VCF + LDhelmet Recombination Rates to EIGENSTRAT format
vcf
linkage
SNP
genome
4.7 years ago by
Jautis
▴ 580
0
votes
0
replies
1.1k
views
find position of snps in cM, given recombination map from ldhelmet
recombination
genome
physical position
4.7 years ago by
Jautis
▴ 580
2
votes
2
replies
2.9k
views
sed (or similar) command to remove part of the FORMAT from a vcf file?
vcf
sed
processing
updated 4.8 years ago by
finswimmer
16k • written 4.8 years ago by
Jautis
▴ 580
1
vote
2
replies
2.0k
views
vcftools minDP filter not working for samtools genotype calling output
genotype filtering
SNP
SNP-calling
5.1 years ago by
Jautis
▴ 580
0
votes
1
reply
1.2k
views
Efficiently run blat for long sequences
blat
alignment
sequence
assembly
updated 5.2 years ago by
Vitis
★ 2.6k • written 5.3 years ago by
Jautis
▴ 580
1
vote
1
reply
1.5k
views
Annotate CpG Islands for a new genome
CpG
assembly
annotation
updated 5.6 years ago by
vkkodali_ncbi
★ 3.8k • written 5.6 years ago by
Jautis
▴ 580
1
vote
8
replies
2.8k
views
Error in transferring annotations to a new assembly using RATT
alignment
annotation
software error
Assembly
updated 5.8 years ago by
h.mon
35k • written 5.9 years ago by
Jautis
▴ 580
2
votes
1
reply
2.7k
views
Create a pseudo-haploid fasta file based genotype calls for an individual (vcf file)
vcf
sequence
assembly
SNP
updated 6.1 years ago by
Len Trigg
★ 1.6k • written 6.1 years ago by
Jautis
▴ 580
0
votes
0
replies
1.1k
views
Find SNPs which disrupt CpG sites
vcf
genome
variants
6.1 years ago by
Jautis
▴ 580
0
votes
0
replies
1.6k
views
Determine the derived allele
alignment
6.3 years ago by
Jautis
▴ 580
1
vote
2
replies
2.9k
views
GOseq with non-supported organism
GO
GOseq
R
6.4 years ago by
Jautis
▴ 580
1
vote
5
replies
1.7k
views
Find chromosomal location of a scaffold
genome
mapping
updated 6.4 years ago by
h.mon
35k • written 6.4 years ago by
Jautis
▴ 580
3
votes
4
replies
3.9k
views
Convert an altered sam file into a bam file
sam
bam
sequencing
7.0 years ago by
Jautis
▴ 580
0
votes
0
replies
1.9k
views
BSMap to Bismark bam file formats
next-gen
sequencing
bam
bisulfite
7.0 years ago by
Jautis
▴ 580
0
votes
2
replies
1.3k
views
Genotype calls for a list of variable sites
genotype-calling
GATK
variant-calling
updated 7.1 years ago by
Pierre Lindenbaum
164k • written 7.1 years ago by
Jautis
▴ 580
10
votes
4
replies
6.4k
views
Comparing two phylogenies
covariance
phylogeny
tree
updated 2.2 years ago by
Ram
44k • written 9.2 years ago by
Jautis
▴ 580
2
votes
3
replies
2.0k
views
Outputting DP4 flag in GATK
variant calling
sequencing
gatk
updated 7.7 years ago by
Santosh Anand
5.8k • written 7.7 years ago by
Jautis
▴ 580
0
votes
7
replies
1.8k
views
Getting reads that end at a digest site from a sam/bam file
bisulfite
digest
updated 7.7 years ago by
Pierre Lindenbaum
164k • written 7.7 years ago by
Jautis
▴ 580
0
votes
1
reply
1.9k
views
Calling allele-specific methylation from bisulfite sequencing reads
bisulfite-sequencing
allele-specific
sequencing
updated 7.8 years ago by
dariober
15k • written 7.8 years ago by
Jautis
▴ 580
5
votes
7
replies
6.2k
views
Downsampling bam file to 2x coverage
bam
sequencing
high-throughput
7.9 years ago by
Jautis
▴ 580
0
votes
1
reply
1.4k
views
high coverage but few genotype calls: possible causes?+
genotype calling
sequencing
SNP
8.5 years ago by
Jautis
▴ 580
3
votes
4
replies
6.2k
views
Compare tree topologies (Newick)
tree
phylogeny
gene
updated 8.8 years ago by
jhc
★ 3.0k • written 8.8 years ago by
Jautis
▴ 580
0
votes
1
reply
1.7k
views
Check for Msp1 digestion in sequencing data
RRBS
digestion
bisulfite-sequencing
msp1
updated 2.4 years ago by
Ram
44k • written 8.9 years ago by
Jautis
▴ 580
0
votes
0
replies
2.6k
views
Genome sites from BPM file
illumina
location
bpm
updated 2.3 years ago by
Ram
44k • written 9.0 years ago by
Jautis
▴ 580
2
votes
2
replies
2.7k
views
Phylogenetic distance betwee species
phylogenetics
newick
trees
updated 2.3 years ago by
Ram
44k • written 9.1 years ago by
Jautis
▴ 580
0
votes
2
replies
2.4k
views
Fst from 012 genotype matrix
Fst
Genotype
updated 2.3 years ago by
Ram
44k • written 9.2 years ago by
Jautis
▴ 580
2
votes
6
replies
3.8k
views
Taking genotypes out of a vcf file
vcf
updated 2.1 years ago by
Ram
44k • written 9.4 years ago by
Jautis
▴ 580
4
votes
3
replies
2.4k
views
Making a haploid genome
vcf
haploid-genome
variant
updated 24 months ago by
Ram
44k • written 9.4 years ago by
Jautis
▴ 580
0
votes
1
reply
2.7k
views
Masking Variable Sites in a Fasta File
fasta
vcf
updated 23 months ago by
Ram
44k • written 9.5 years ago by
Jautis
▴ 580
0
votes
1
reply
3.0k
views
Finding differences between 2 fasta files
fasta
updated 23 months ago by
Ram
44k • written 9.5 years ago by
Jautis
▴ 580
6
votes
4
replies
2.8k
views
Help simulating RRBS reads
methylation
RRBS
updated 23 months ago by
Ram
44k • written 9.5 years ago by
Jautis
▴ 580
7
votes
5
replies
2.6k
views
Filter fastq file by first two base pairs
fastq
updated 22 months ago by
Ram
44k • written 9.6 years ago by
Jautis
▴ 580
6
votes
2
replies
1.6k
views
Comparing methods to genotype
RNA-Seq
genotyping
vcf
RRBS
updated 2.4 years ago by
Ram
44k • written 9.6 years ago by
Jautis
▴ 580
1
vote
6
replies
3.5k
views
Calling SNPs from RRBS data
SNP
RRBS
SNP-calling
bisulfite-sequencing
updated 2.6 years ago by
Ram
44k • written 9.8 years ago by
Jautis
▴ 580
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