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1,000 results • Page
1 of 20
Sort: Views
Rank
Views
Votes
Replies
23
votes
22
replies
37k
views
6 follow
Converting VCF to PLINK .bed binary fileset to check for pedigree errors with KING: How do conversion tools make the PLINK .fam file, without asking …
plink
vcf
fam
gatk
vcftools
updated 3 months ago by
Nicole
• 0 • written 4.9 years ago by
gaelgarcia
▴ 250
19
votes
15
replies
25k
views
8 follow
Converting SNP from chr:pos to rs number using PLINK?
plink
SNP
updated 7 months ago by
Ram
38k • written 7.2 years ago by
dam4l
▴ 180
4
votes
13
replies
24k
views
6 follow
[main_samview] fail to read the header from sample.bam
alignment
updated 8 months ago by
Qboy
• 0 • written 5.0 years ago by
sambioinfo2018
▴ 20
2
votes
8
replies
16k
views
Using vcfutils.pl command
alignment
updated 11 months ago by
Ram
38k • written 8.1 years ago by
lcc1844
▴ 40
16
votes
38
replies
15k
views
Differential gene Analysis by Limma
Limma
Microarray
R
updated 11 months ago by
Ram
38k • written 8.1 years ago by
Mo
▴ 920
0
votes
3
replies
14k
views
How to choose a TPM cut-off point
RNA-Seq
transcript
tpm
updated 7 months ago by
Ram
38k • written 7.4 years ago by
amyfm
▴ 10
2
votes
4
replies
14k
views
TRIMMOMATRIC Nextera trimming
next-gen
updated 5 months ago by
Ram
38k • written 7.6 years ago by
meekadi
▴ 10
1
vote
8
replies
13k
views
HTSeq-count high number of no_feature
htseq-count
rna-seq
updated 11 months ago by
Ram
38k • written 8.1 years ago by
cafelumiere12
▴ 80
0
votes
4
replies
12k
views
Unable to install XLconnect package in R studio version 3.2.1
R
updated 5 months ago by
Ram
38k • written 7.6 years ago by
Debbie
▴ 10
3
votes
11
replies
12k
views
What is the acceptable % of reads that map to no feature (in RNASeq)?
htseq
RNA-Seq
STAR
updated 11 months ago by
Ram
38k • written 8.2 years ago by
noushin.farnoud
▴ 120
2
votes
4
replies
12k
views
Run BLAST on Linux terminal
ncbi
nBLAST
linux
blast
updated 6 months ago by
Ram
38k • written 7.5 years ago by
Abdul Rafay Khan
★ 1.2k
8
votes
5
replies
11k
views
samtools tview symbols
samtools
updated 4 months ago by
Ram
38k • written 7.7 years ago by
biolab
★ 1.4k
0
votes
4
replies
10k
views
Convert .gbf file to .gbk or .gff
gbk
gff
gbf
updated 8 weeks ago by
Ram
38k • written 7.8 years ago by
che.bellaj
• 0
2
votes
3
replies
10k
views
converting maf to vcf
Exome
maf2vcf
updated 8 weeks ago by
Ram
38k • written 7.8 years ago by
ashishchahl
• 0
3
votes
1
reply
10k
views
Negative P-Values
gene
genome
next-gen-sequencing
updated 7 months ago by
Ram
38k • written 7.5 years ago by
stevenlang123
▴ 200
2
votes
0
replies
10k
views
How to plot UniFrac PCoA with 95% confidence Elipses in R
metagenomics
ordiellipse
vegan
R
phyloseq
updated 12 months ago by
Ram
38k • written 8.2 years ago by
c.v.oflynn
▴ 100
0
votes
0
replies
9.2k
views
pheatmap row annotation and title font size questions
heatmap
pheatmap
updated 10 weeks ago by
Ram
38k • written 7.8 years ago by
neokao
• 0
3
votes
6
replies
9.2k
views
6 follow
How to calculate genetic correlation with R
R
updated 10 months ago by
ibomsolomon
• 0 • written 8.9 years ago by
Tohamy
▴ 80
1
vote
6
replies
8.4k
views
How to use python to process .CEL file?
cel
affymetrix
python
R
cmap
updated 10 months ago by
Ram
38k • written 8.0 years ago by
zero_hsy
▴ 110
4
votes
6
replies
8.4k
views
Spades assembler output
Assembly
updated 7 months ago by
Ram
38k • written 7.2 years ago by
elbecerrasoto
▴ 30
4
votes
3
replies
8.3k
views
Convert Tab delimited file to VCF file
snp
updated 9 months ago by
Ram
38k • written 7.4 years ago by
niharraul
• 0
10
votes
11
replies
8.2k
views
How to adjust my manhattan plot to look better?
qqman
manhattan
R
updated 9 months ago by
Ram
38k • written 8.0 years ago by
SheelS
▴ 40
18
votes
4
replies
8.0k
views
How To Find Rna-Seq Data Of Published Papers?
geo
next-gen
RNA-seq
updated 22 days ago by
Ram
38k • written 9.6 years ago by
user
▴ 930
3
votes
8
replies
8.0k
views
Quantile normalizing prior to or after TPM scaling?
RNAseq
normalization
updated 5 weeks ago by
Kevin Blighe
84k • written 5.3 years ago by
mforde84
★ 1.4k
2
votes
2
replies
7.8k
views
How to filter out special sequences from a fasta file based on sequence IDs txt
fasta
updated 6 months ago by
Ram
38k • written 7.5 years ago by
Ginsea Chen
▴ 130
5
votes
4
replies
7.8k
views
GFF3 to GTF conversion - 9th column
gtf
NCBI
gff3
featureCounts
updated 7 months ago by
Ram
38k • written 7.2 years ago by
mrodrigues.fernanda
▴ 50
2
votes
7
replies
7.7k
views
linux 'cat' command merge fasta files without headers
fasta
linux
updated 15 days ago by
Ram
38k • written 8.8 years ago by
esterbuiate
• 0
1
vote
2
replies
7.6k
views
vcf compare between 2 vcf files using vcf tools
vcftools
updated 8 days ago by
Ram
38k • written 6.3 years ago by
bioguy24
▴ 220
2
votes
1
reply
7.5k
views
ROH by PLINK
plink
ROH
updated 5 weeks ago by
Ram
38k • written 7.9 years ago by
afadda
▴ 20
1
vote
2
replies
7.2k
views
Converting vcf to fasta format
fasta
samtools
vcf
alignment
next-gen
updated 3 months ago by
Ram
38k • written 7.7 years ago by
JW
▴ 10
3
votes
7
replies
7.2k
views
RNA-STAR, mapping problem (number of reads)
RNA-Seq
updated 8 months ago by
Ram
38k • written 7.1 years ago by
mohikran
• 0
4
votes
2
replies
6.9k
views
PLINK Merge error: File write failure
plink
1000genomes
updated 6 months ago by
Ram
38k • written 7.4 years ago by
aritra90
▴ 70
1
vote
6
replies
6.7k
views
using bcftools/samtools to generate consensus using reference + variants; output is a truncated reference
samtools
bcftools
mosaik
consensus
rc454
updated 10 months ago by
Ram
38k • written 8.0 years ago by
nirvan
▴ 10
2
votes
7
replies
6.7k
views
Bowtie2 run out of memory
software-error
alignment
bowtie2
updated 6 weeks ago by
Ram
38k • written 7.9 years ago by
anon
▴ 50
0
votes
0
replies
6.7k
views
Error in grid.Call.graphics(L_setviewport, vp, TRUE) : non-finite location and/or size for viewport
gviz
updated 8 months ago by
Ram
38k • written 7.5 years ago by
nasim.zeeshan25
• 0
3
votes
5
replies
6.6k
views
Visualising the number of overlapping peaks in ChIP-seq studies
ChIP-Seq
updated 8 months ago by
Ram
38k • written 7.1 years ago by
James Ashmore
★ 3.4k
0
votes
10
replies
6.6k
views
Error: reads file does not look like a fastq file
fastq
bowtie2
ChIP-Seq
updated 4 days ago by
Ram
38k • written 6.5 years ago by
addilynn.beach
▴ 40
6
votes
3
replies
6.6k
views
How to set a threshold for coefficient of variation in RNA-seq?
dispersion
statistics
single-cell
RNA-Seq
variance
updated 11 months ago by
Ram
38k • written 8.2 years ago by
gaelgarcia
▴ 250
2
votes
5
replies
6.5k
views
Tophat Protocol Error Occured At Step 4
tophat
rna-seq
updated 10 months ago by
Ram
38k • written 10.8 years ago by
ashis.csedu
▴ 100
0
votes
2
replies
6.5k
views
Illumina adapter diagram
illumina
sequencing
adapter-trimming
updated 8 months ago by
Ram
38k • written 7.9 years ago by
pjkriebel
• 0
5
votes
22
replies
6.4k
views
SVM for classified gene expression data
R
svm
microarray
updated 7 months ago by
Ram
38k • written 7.2 years ago by
Shaurya Jauhari
▴ 50
3
votes
5
replies
6.3k
views
Converting Vcftools output to R readable format
vcf
SNP
R
vcftools
updated 8 weeks ago by
Ram
38k • written 7.8 years ago by
pifferdavide
▴ 100
5
votes
11
replies
6.3k
views
Error while running miso
RNA-Seq
splicing
updated 7 months ago by
Ram
38k • written 7.6 years ago by
priyankamaripuri
▴ 40
10
votes
5
replies
6.3k
views
how to remove asterisk characters from a translated sequences (fasta format)?
sequencing
Assembly
alignment
updated 7 months ago by
Ram
38k • written 7.6 years ago by
seta
★ 1.8k
4
votes
8
replies
6.3k
views
Error while demultipleaxing .bcl to .fastq files
sequencing
genome
alignment
updated 6 months ago by
Ram
38k • written 7.5 years ago by
ravi.uhdnis
▴ 220
0
votes
0
replies
6.3k
views
E-values calculation (MEME)
meme
updated 8 weeks ago by
Ram
38k • written 7.8 years ago by
anahochmanova
▴ 10
0
votes
3
replies
6.2k
views
Cross validation error Admixture
SNP
software-error
updated 10 months ago by
Ram
38k • written 8.0 years ago by
benhalimayossra
• 0
2
votes
3
replies
6.2k
views
bwa mem failed to allocate memory
bwa-mem
bwa
updated 11 months ago by
Ram
38k • written 8.2 years ago by
cmo
▴ 90
3
votes
2
replies
6.0k
views
Hypergeometric test of gene set enrichment - Calculate P-value for multiple gene sets in one script?
next-gen
R
GO
updated 11 months ago by
Ram
38k • written 8.1 years ago by
nsilmondemonerri
▴ 20
1
vote
8
replies
6.0k
views
Plotting different gene ontology categories in a barplot
HI
Gene ontology
R
updated 7 months ago by
zx8754
11k • written 2.1 years ago by
aradhana
• 0
1,000 results • Page
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Can I sort my bam files with Picard MergeSamFiles?
Answer: Problem generating a .vcf after upgrade of samtools and bcftools
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Comment: activity of unloaded/unassembled Tn5
by
callumjcparr
• 0
![enter image description here][1] enter image description here ![enter image description here][2] [1]: /media/images/d06e761c-b715…
Answer: How to implement this two-stage one-to-many workflow using WDL?
by
Ruben
• 0
> Unfortunately, as far as I can tell, WDL provides no support for iterating over the contents of a directory. (I find this shocking. I con…
Answer: activity of unloaded/unassembled Tn5
by
callumjcparr
• 0
So I hope someone is still interested in this. We have taken to preparing recombinant Tn5 now as it's much cheaper than commercial suppli…
Comment: RNA-SEQ
by
ali
• 0
thanks for your helping
Comment: TSS of protein coding genes
by
ConvolutedGenome
▴ 10
I am quite confused with GENCODE GTF file, So, within the GENCODE GTF file, I noticed that each (protein-coding) gene has multiple "transc…
Comment: Recommendation for (Alternative) Splicing analysis packages for bulk RNA-seq da
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5.8k
Hi! I personally use [SplAdder][1], in case you want to add it to your list :). [1]: https://github.com/ratschlab/spladder
Answer: Problem generating a .vcf after upgrade of samtools and bcftools
by
Andy
• 0
Really the only needed, that help worked, thank's
Comment: Active enhancers for mm39
by
seidel
11k
Just curious what you mean by "active" enhancers. Enhancers are active in a given context (e.g. cell type developmental state, etc.), and m…
Comment: Creating loop for read groups using Picard
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ntsopoul
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try absolute paths navigate to the directory with cd and use pwd to get the absolute directory.
Comment: how to create interacting Hi-C peaks
by
rheab1230
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Thank you. I will use this package since I am more familiar with R
Comment: how to create interacting Hi-C peaks
by
rheab1230
▴ 140
thank you. i will go through it
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by
npavliukovec
• 0
Yeah, after trimming and fastqc I will have to generate MultiQC plots and after do mapping with reference genome. As I know, for eukaryotes…
Comment: My fastq files(paired end) have different read number
by
kimgeng
• 0
Oh, I see, Thank you however, I want to make vcf files with gatk haplotypecaller and GenotypeGVCFs. But I got some problems I have about 2.…
Answer: My fastq files(paired end) have different read number
by
ntsopoul
▴ 20
Yes, this is normal because depending on how you generate the bam file, the non-aligning reads are saved in the .bam file along the properl…
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by
ntsopoul
▴ 20
No, you should not do that since the count matrix is not normalized. Also, the statistics for getting a pValue requires consideration of al…
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