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Showing :
questions
2
votes
6
replies
809
views
What is the expected number of common/mutual/shared SNVs between two, three, four... unrelated individuals?
snv
genomics
variation
snp
human
10 weeks ago by
Joel Wallenius
▴ 210
4
votes
8
replies
1.3k
views
Locating IBD candidates with just VCF files
Relatedness
Genotypes
IBD
Haplotypes
VCF
10 weeks ago by
Joel Wallenius
▴ 210
0
votes
1
reply
463
views
GATK's CNV-caller output, genotype code?
GATK
CNV
NGS
updated 3 months ago by
Rui Xu
• 0 • written 20 months ago by
Joel Wallenius
▴ 210
0
votes
6
replies
737
views
Parallel GWAS?
GWAS
Parallel
Chromosome
updated 10 months ago by
zx8754
11k • written 10 months ago by
Joel Wallenius
▴ 210
2
votes
4
replies
720
views
Upstream pseudogene causing MAPQ 0 and exclusion during variant calling
Mapping
Variant-calling
masking
updated 10 months ago by
GenoMax
142k • written 11 months ago by
Joel Wallenius
▴ 210
0
votes
0
replies
381
views
What are the WES-specific settings when running GATK's variant recalibration step?
WES
GATK
recalibration
exome
12 months ago by
Joel Wallenius
▴ 210
0
votes
0
replies
335
views
A program that detects similar regions between samples in a multi-sample VCF file?
Relatedness
IBD
Haplotypes
18 months ago by
Joel Wallenius
▴ 210
0
votes
0
replies
281
views
How many SNPs are needed to perform haplotype analysis on siblings and their mother?
haplotype
linkage
SNP
pedigree
18 months ago by
Joel Wallenius
▴ 210
2
votes
22
replies
2.3k
views
6 follow
Find ~1 Mb regions of genome that are shared by two or more WGS samples?
pedigree
linkage
genetics
18 months ago by
Joel Wallenius
▴ 210
5
votes
6
replies
1.1k
views
Can you not phase exome data?
phasing
shapeit
wes
exome
beagle
updated 20 months ago by
LauferVA
4.2k • written 20 months ago by
Joel Wallenius
▴ 210
2
votes
2
replies
755
views
How to properly subset a bam file?
bam
subset
truncate
20 months ago by
Joel Wallenius
▴ 210
6
votes
7
replies
1.9k
views
Convert a BAM from GRCh37 to hg19?
GRCh37
hg19
BAM
updated 21 months ago by
Ram
43k • written 22 months ago by
Joel Wallenius
▴ 210
0
votes
0
replies
344
views
STR expansion detection on IonTorrent WES data?
repeat
STR
IonTorrent
wes
ngs
short
tandem
22 months ago by
Joel Wallenius
▴ 210
0
votes
0
replies
366
views
"Best" freewares for linkage analyses?
Equilibrium
Linkage
Disequilibrum
haplotyping
22 months ago by
Joel Wallenius
▴ 210
4
votes
11
replies
1.4k
views
Bam file to Sanger-like chromatogram?
sanger
visualization
diagram
plot
bam
2.1 years ago by
Joel Wallenius
▴ 210
3
votes
9
replies
1.2k
views
RC an entire bam file?
sam
genome
complement
viewer
alignment
bam
Reverse
2.1 years ago by
Joel Wallenius
▴ 210
3
votes
10
replies
2.2k
views
Mate pairs and paired reads confusion
sequencing
2.1 years ago by
Joel Wallenius
▴ 210
0
votes
0
replies
416
views
Alternatives to ExpansionHunter?
Repeat
STR
Expansion
Genetics
Repeats
2.2 years ago by
Joel Wallenius
▴ 210
2
votes
4
replies
1.7k
views
GATK's GenomicsDBImport takes forever...
Variant
GATK
Calling
2.6 years ago by
Joel Wallenius
▴ 210
0
votes
8
replies
1.3k
views
Best alignment software for mapping short DNA reads to transcriptome?
alignment
Transcriptome
DNA
4.3 years ago by
Joel Wallenius
▴ 210
20
votes
26
replies
3.2k
views
Is there a command line tool that can take an alignment fasta and input and outputs an image?
alignment
fasta
image
updated 9 months ago by
Joe
21k • written 4.9 years ago by
Joel Wallenius
▴ 210
0
votes
0
replies
765
views
AnnoVar with custom genomes?
AnnoVar
Annovar
4.9 years ago by
Joel Wallenius
▴ 210
0
votes
9
replies
5.4k
views
Calculating FPKM and TPM by hand from htseq-count output?
RNA-Seq
rna-seq
htseq
FPKM
TPM
updated 9 months ago by
ATpoint
82k • written 5.1 years ago by
Joel Wallenius
▴ 210
2
votes
7
replies
1.4k
views
Where is the (hg19) reference data for transcript isoforms' relative abundances for each gene?
RNA-Seq
transcriptomics
isoforms
updated 5.0 years ago by
i.sudbery
19k • written 5.0 years ago by
Joel Wallenius
▴ 210
1
vote
19
replies
2.0k
views
Approximately following the GATK recommended workflow for DNA sequence data, my mpileup output files are empty
sequencing
SNP
genome
next-gen
5.1 years ago by
Joel Wallenius
▴ 210
2
votes
5
replies
1.5k
views
Given a list of RefSeq homo sapiens mRNA transcripts, what is the simplest way to get the corresponding sequences from some other related species?
alignment
transcriptome
orthology
6.1 years ago by
Joel Wallenius
▴ 210
2
votes
1
reply
1.1k
views
Interpreting the output of an mRNA structural motif search algorithm
mRNA
motif
structure
updated 6.3 years ago by
Martombo
★ 3.1k • written 6.3 years ago by
Joel Wallenius
▴ 210
0
votes
2
replies
1.4k
views
Given a protein domain, like a TPR or zinc finger or some other one, can you predict what RNA sequence it binds to?
RNA
RBP
Protein
Affinity
6.3 years ago by
Joel Wallenius
▴ 210
0
votes
11
replies
3.1k
views
Getting MPI to work with MEME suite CPU parallelization in OpenSuse
meme
mpi
parallelization
opensuse
updated 6.4 years ago by
Alex Reynolds
35k • written 6.4 years ago by
Joel Wallenius
▴ 210
0
votes
4
replies
1.3k
views
Find all nuclear genes the mRNA of which binds to the CLUH protein for transport to mitochondria?
mitochondria
mRNA
transport
CLUH
updated 6.5 years ago by
Jeremy Leipzig
22k • written 6.5 years ago by
Joel Wallenius
▴ 210
0
votes
6
replies
3.5k
views
The meaning of '0' allele frequency in vcftools output
vcf
vcftools
MAF
allele frequency
allele
updated 6.6 years ago by
Biostar
20 • written 6.6 years ago by
Joel Wallenius
▴ 210
2
votes
8
replies
2.5k
views
Imposing a human reference genome onto a vcf file?
vcf
genome
sequencing
SNP
allele
updated 6.6 years ago by
Pierre Lindenbaum
161k • written 6.6 years ago by
Joel Wallenius
▴ 210
32 results • Page
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