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121,922 results • Page
717 of 2439
Sort: Rank
Rank
Views
Votes
Replies
0
votes
1
reply
1.5k
views
Making PLINK compatible files from VCF file without phenotype information
plink
gwas
vcf
4.6 years ago by
mfshiller
▴ 20
1
vote
2
replies
1.8k
views
Trying to get sequence using sequinr generates error "Error in readLines(socket, n = nelem, ok = FALSE)"
gene
software error
sequence
R
genome
4.6 years ago by
poecile.pal
▴ 50
4
votes
7
replies
2.3k
views
Chunk That Fasta?
FASTA
Python
Chunk
DNA Sequence
updated 4.6 years ago by
Biostar
20 • written 5.9 years ago by
damonlbp
▴ 20
23
votes
6
replies
16k
views
7 follow
Bioinformatics Journal with no publishing fees?
Journal
updated 2.5 years ago by
Ram
45k • written 10.9 years ago by
Abdul Rafay Khan
★ 1.2k
0
votes
4
replies
1.2k
views
multi platform GEO analysis based in expression of one gene
geo analysis
microarray analysis
geo
R
written 4.6 years ago by
amirnavidinia2014
▴ 10
2
votes
6
replies
4.3k
views
PRSice: how to obtain exact list of SNPs used for PRSice.best
PRS
PRSice
PLINK
updated 2.7 years ago by
Sam
★ 4.8k • written 5.0 years ago by
m98
▴ 440
2
votes
7
replies
2.6k
views
Annotate hs37d5 genome calls using VEP
vep
annotation
1kgenomes
hs37d5
written 5.3 years ago by
igor
• 0
0
votes
1
reply
668
views
Find SNPs common to mutants, absent in WT (vcf files)
vcf
bcftools
written 4.6 years ago by
charlesh
• 0
2
votes
6
replies
1.4k
views
GMAP intron control
GMAP
mapping
cDNA
intron
written 4.6 years ago by
ch-h
• 0
1
vote
1
reply
918
views
SRA screening for parasite contamination
blast
data screening
rRNA
parasite
host
updated 4.6 years ago by
Mensur Dlakic
★ 30k • written 4.6 years ago by
e.bessette
▴ 10
0
votes
0
replies
757
views
copy number variation, fisher exact test, gistic2.0
gene
genome
4.6 years ago by
Rob
▴ 180
1
vote
8
replies
1.5k
views
Vcf file extraction
SNP
next-gen
updated 4.6 years ago by
Biostar
20 • written 4.6 years ago by
C4
▴ 30
0
votes
1
reply
705
views
MARVEL all_vogs_hmm_profiles issue
MARVEL
prophage
phage
genomics
updated 4.6 years ago by
Mensur Dlakic
★ 30k • written 4.6 years ago by
ams686
• 0
5
votes
1
reply
680
views
Assigning a new value to a function being called on a variable
R
4.6 years ago by
angus.j.g.campbell
▴ 10
0
votes
0
replies
533
views
Bowtie2 alignment accuracy
alignment
mapping
4.6 years ago by
anabaena
▴ 10
1
vote
1
reply
4.8k
views
Python Script To Do Virtual Screening On Pyrx
pyrx
autodock
updated 2.5 years ago by
Ram
45k • written 13.5 years ago by
Onat
▴ 40
0
votes
11
replies
2.0k
views
Bulk transcriptome RNA-Seq dataset of Human breast cancer
RNA-Seq
rna-seq
dataset
human breast cancer
4.6 years ago by
H. Z. Amini
• 0
0
votes
0
replies
655
views
Population Genetics WGS: how do I know if I have too few individuals?
wgs
sequencing
next-gen
4.6 years ago by
timothy.delory
▴ 20
3
votes
7
replies
14k
views
Seurat Clustering - Cluster Numbers from 1 instead of 0
RNA-Seq
seurat
Cluster
numbering
updated 4.6 years ago by
pjlmac
• 0 • written 5.2 years ago by
David_emir
▴ 500
0
votes
0
replies
1.4k
views
Displaying a controversial phylogenetic tree as a network to explicitate noise-generating branches
phylogenetic-tree
network
genome
updated 2.2 years ago by
Ram
45k • written 7.2 years ago by
Matteo Schiavinato
★ 3.7k
0
votes
0
replies
930
views
Compare fold change and p values for the same gene between different DESeq runs
RNA-Seq
DESeq
R
volcano
single cell
4.6 years ago by
kw486
▴ 50
2
votes
3
replies
975
views
Very strange duplicate output with stand alone blast
BLAST
4.6 years ago by
Firingam
▴ 30
0
votes
5
replies
1.1k
views
How to search for similar sequences in all public metagenomes?
metagenome
updated 4.6 years ago by
Mensur Dlakic
★ 30k • written 4.6 years ago by
Dgg32
▴ 90
0
votes
0
replies
694
views
how to convert ped files to cnv
convertit
cnv
ped
4.6 years ago by
iag.14800108
• 0
0
votes
0
replies
426
views
How to do Annotate the with allele frequency?
genome
alignment
SNP
4.6 years ago by
mvahed
• 0
0
votes
1
reply
1.7k
views
Job:
Fully Funded Doctoral Researcher Position in Data Science & Health
data-science
updated 2.3 years ago by
Ram
45k • written 6.6 years ago by
sichr2
▴ 10
4
votes
3
replies
5.7k
views
Pruning a VCF file and extracting pruned in snps using bcftools
bcftools
SNP
updated 2.3 years ago by
Ram
45k • written 4.6 years ago by
AVA
▴ 40
0
votes
0
replies
924
views
How to subsample SARS-CoV-2 dataset with limited computational resources?
sars-cov-2
subsample
ram
genome
gisaid
4.6 years ago by
fhsantanna
▴ 620
4
votes
8
replies
2.7k
views
Unused argument in R
R
4.6 years ago by
paria
▴ 110
2
votes
8
replies
4.4k
views
Why sortmerna 4.2.0 runs so slow?
RNA-Seq
sortmerna
software error
RNA
rna-seq
updated 4.6 years ago by
Nifaste
▴ 20 • written 5.4 years ago by
tianshenbio
▴ 190
0
votes
1
reply
4.1k
views
rfe function from caret to perform svm-rfe feature selection
R
feature selection
caret
rfe
svm
updated 4.6 years ago by
tzehuey85
• 0 • written 4.9 years ago by
lenC_biotecLover
▴ 90
0
votes
4
replies
909
views
Finding TBP binding sites on Chipseq Data
ChIP-Seq
4.6 years ago by
majeedmj.ict
▴ 20
0
votes
8
replies
1.7k
views
How to split .bed file in R
r
rna-seq
genome
4.6 years ago by
vivianbalagon
• 0
1
vote
3
replies
898
views
Getting matched peptide to CDR3 sequences
RNA-Seq
4.6 years ago by
zizigolu
★ 4.4k
1
vote
6
replies
3.4k
views
DESEq2 error - 'DESeqDataSet' object superclass 'RectangularData' not defined in the environment of the object's class
DESeq2
R
DESeq
updated 4.6 years ago by
Michael Love
★ 2.6k • written 4.7 years ago by
susheelbhanu
• 0
2
votes
2
replies
7.7k
views
Error attaching phenotype in PLINK (fewer tokens than expected)
GWAS
PLINK
4.6 years ago by
absoldini
▴ 10
21
votes
7
replies
27k
views
Kmer Content in FastQC failed
next-gen-sequencing
updated 3.2 years ago by
Ram
45k • written 9.7 years ago by
hurtc.stri
▴ 20
0
votes
0
replies
1.1k
views
WGCNA: how eigengene expression calculated?
wgcna
sequencing
RNA-Seq
4.6 years ago by
Shero
▴ 10
0
votes
0
replies
578
views
CONTRA OUTPUT FILE (GENE.SYM -UNKNOWN)
CNV Calling
Targeted Sequencing
4.6 years ago by
sushumitha6
• 0
0
votes
1
reply
639
views
Can you average values to do WGCNA?
RNA-Seq
WGCNA
R
Gene Network
4.6 years ago by
gerastuff
• 0
0
votes
0
replies
872
views
recover IMG ids from JGI site
JGI
IMG
ids
updated 4.6 years ago by
lieven.sterck
15k • written 4.6 years ago by
sapuizait
▴ 10
1
vote
1
reply
976
views
Bionano Saphyr Structural Variant ID and Genome Assembly
Assembly
genome
updated 2.5 years ago by
Ram
45k • written 4.6 years ago by
dk0319
▴ 70
4
votes
1
reply
1.6k
views
Are there any repository for panel of normal for running Mutect2?
Mutect2
PON
panel of normal
gatk
4.6 years ago by
DareDevil
★ 4.4k
2
votes
2
replies
1.1k
views
Maker Annotation - multiple gene models give same blastp match
genome
annotation
Maker
updated 4.6 years ago by
lieven.sterck
15k • written 4.6 years ago by
MH85
▴ 20
0
votes
0
replies
535
views
Converting VCF file to ms-style output
SNP
genome
sequence
4.6 years ago by
Jamie Watson
▴ 10
0
votes
9
replies
1.5k
views
for loop command
for loop
fasta
updated 4.6 years ago by
lieven.sterck
15k • written 4.6 years ago by
harry
▴ 40
4
votes
6
replies
2.1k
views
GWAS missing p-values
software error
snp
genome
GWAS
logistic regression
updated 4.6 years ago by
hkj7
• 0 • written 6.7 years ago by
emmacomp
▴ 10
0
votes
1
reply
959
views
Database of drugs warnings/risk
DrugBank
database
risk rating
warning
4.6 years ago by
annydisomma20
• 0
0
votes
0
replies
699
views
exomePeak for non-fragmented libraries
exomePeak
4.6 years ago by
blur
▴ 280
1
vote
7
replies
4.9k
views
Using the Homer suite with conda
homer
conda
bioconda
updated 4.6 years ago by
Biostar
20 • written 8.3 years ago by
rioualen
▴ 750
121,922 results • Page
717 of 2439
Recent Votes
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A: read.table does not read in all rows!
A: Binning Over Genes And Calculating The Coverage [Bedops/Bedmap]
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Comment: miRNA low mapping ratings
by
Ant
▴ 50
Sorry, I gave you answers based on different samples. The thing is, the total number of reads is very low (around 1–10% of the total reads)…
Comment: miRNA low mapping ratings
by
Ant
▴ 50
Yes, it was in 75bp. I don1t know if it was the first time he used the kit, but I remember he needs to adjust the protocol.
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by
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153k
> Is it possible to do this at the assembly level? By aligning to a reference you can find the differences between your assembly and the …
Comment: miRNA low mapping ratings
by
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22k
4bp would suggest there was nothing cloned into the library. But i'm a bit confused. In example in the question, it talks about 50,000 re…
Comment: miRNA low mapping ratings
by
GenoMax
153k
> while fewer than 100,000 reads were around 18-22 bp. That is why are you likely seeing the numbers you are observing in alignments. Wa…
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by
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22k
I would imagine this is something one of the AI code tools could handle.
Comment: cellranger mkref fail/error
by
ATpoint
89k
I think OCM = https://www.10xgenomics.com/support/software/cell-ranger/latest/getting-started/cr-3p-what-is-cellplex#on-chip Seconding to…
Comment: miRNA low mapping ratings
by
Ant
▴ 50
The first one it's the results from Cutadapter and the second block from miRDeep2.
Comment: miRNA low mapping ratings
by
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▴ 50
Thanks for the reply, when running: cutadapt -a AACTGTAGGCACCATCAAT -M 30 -o example_trimmed.fastq.gz data/xxx.fastq.gz, the sequence le…
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153k
> I don’t have clear species labels in my headers, only sequence IDs. I have not used iqtree, so this is only a thought ... should it be y…
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Thank you so much.
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Yes, it seems so. Thank you.
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153k
> The thing is that I do not have a genome for these organisms. That is not what `cellranger mkref` is expecting. You could consider alt…
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The thing is that I do not have a genome for these organisms. i made a transcriptome using TRinity and this is what I am feeding it. I do n…
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Hi, I am not sure if i can call them good assemblies. Although based on QUAST and BUSCO stats, everything looks too good but somehow i hav…
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