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1,000 results • Page
3 of 20
Sort: Views
Rank
Views
Votes
Replies
6
votes
8
replies
10k
views
7 follow
Converting SNP names from Illumina GSA array to rsID using PLINK
SNP
plink
6.5 years ago by
dam4l
▴ 200
4
votes
6
replies
9.9k
views
Spades assembler output
Assembly
updated 20 months ago by
Ram
43k • written 8.3 years ago by
elbecerrasoto
▴ 30
0
votes
8
replies
9.9k
views
how to find a read by name in a bam file
next-gen-sequencing
updated 9 months ago by
Ram
43k • written 6.8 years ago by
himanimalhotra89
• 0
3
votes
10
replies
9.9k
views
How can I obtain SNP from TCGA?
Risky-allele
BRCA
SNP
updated 2.3 years ago by
Ram
43k • written 9.6 years ago by
purmod
▴ 10
3
votes
5
replies
9.8k
views
pheatmap: how to avoid fontface, fontsize, and color from writing over existing rownames
fontsize
rows
color
R
pheatmap
updated 2.9 years ago by
cpad0112
21k • written 2.9 years ago by
ladypurrsia
▴ 60
0
votes
2
replies
9.8k
views
DESeq2 pheatmap returns Error in check.length("fill") : 'gpar' element 'fill' must not be length 0
RNA-Seq
DESeq2
gpar
pheatmap
6.5 years ago by
Anthony.Knox
▴ 60
2
votes
2
replies
9.8k
views
Multiple whole genome alignment tools ?
multiple whole genome
alignment
4.9 years ago by
Picasa
▴ 640
11
votes
29
replies
9.7k
views
SummarizedExperiment nrow differs from ncol
DESeq2
SummarizedExperiment
updated 2.5 years ago by
Ram
43k • written 9.9 years ago by
Parham
★ 1.6k
0
votes
4
replies
9.7k
views
How to install PLINK on linux/Mac-OS
genome
3.4 years ago by
giusdalt95
▴ 10
4
votes
10
replies
9.7k
views
Questions about multithreading of BWA
bwa
multithread
updated 5.6 years ago by
Ram
43k • written 8.2 years ago by
michealsmith
▴ 790
1
vote
4
replies
9.7k
views
R ggplot Align Y-Axis on multiple graphs
ggarrange
ggplot2
r
updated 4.7 years ago by
Biostar
20 • written 6.2 years ago by
jjrin
▴ 40
1
vote
13
replies
9.7k
views
MDS Plot R
RNA-Seq
4.8 years ago by
BioBaby
▴ 20
4
votes
3
replies
9.6k
views
Convert Tab delimited file to VCF file
snp
updated 22 months ago by
Ram
43k • written 8.5 years ago by
niharraul
• 0
1
vote
6
replies
9.6k
views
How to use python to process .CEL file?
cel
affymetrix
python
R
cmap
updated 23 months ago by
Ram
43k • written 9.1 years ago by
zero_hsy
▴ 110
2
votes
17
replies
9.6k
views
7 follow
EXITING: because of fatal INPUT file error: could not open read file
mapping
genome
fastq
STAR
updated 2.1 years ago by
todd.ugine
• 0 • written 3.3 years ago by
merfer0206
• 0
5
votes
11
replies
9.5k
views
R- Kruskal-Wallis test on multiple columns at once
R
statistics
test
kruskal-Wallis
R-statistics
4.7 years ago by
mafernandez
• 0
0
votes
19
replies
9.5k
views
Skip orientation as there are not enough pairs by bwa mem
whole genome
bwa
paired end sequencing
4.9 years ago by
seta
★ 1.9k
3
votes
8
replies
9.5k
views
topTable in limma
limma
toptable
6.5 years ago by
AHW
▴ 90
3
votes
9
replies
9.5k
views
Random Forest returns "New factor levels not present in the training data"
R
Machine Learning
microarrays
6.2 years ago by
arronar
▴ 280
3
votes
5
replies
9.5k
views
Using 'blastn' to do a remote search on NCBI BLAST against the nt collection database
blast
shell
unix
linux
6.2 years ago by
maciwuk
• 0
1
vote
6
replies
9.5k
views
Deseq2 : Filtering low counts before per sample
Deseq2
threshold-seq
5.4 years ago by
Cdk
• 0
2
votes
2
replies
9.5k
views
Imputation Analysis In Plink?
plink
gwas
imputation
12.1 years ago by
Davy
▴ 210
3
votes
7
replies
9.4k
views
6 follow
remote blast requires installation of taxdb database
blast
updated 4.9 years ago by
Varshney
▴ 20 • written 6.5 years ago by
hfan22
▴ 40
7
votes
5
replies
9.4k
views
strange issues with absent EOF markers in BAM files
samtools
picard-tools
bam
eof
7.9 years ago by
abascalfederico
★ 1.2k
4
votes
2
replies
9.4k
views
Hisat2 versus Bowtie2
Exome-sequencing
hisat2
bowtie2
updated 6.8 years ago by
Biostar
20 • written 8.0 years ago by
nalpas.nicolas
▴ 20
2
votes
12
replies
9.4k
views
8 follow
michigan imputation server
conversion
michigan imputation server
updated 2.4 years ago by
Fazil
• 0 • written 6.1 years ago by
Teresa
▴ 20
2
votes
7
replies
9.4k
views
How to annotate TTS or TES
ChIP-Seq
TES
annotation
7.2 years ago by
Lila M
★ 1.2k
0
votes
11
replies
9.3k
views
Error in installation R package
R
updated 7.6 years ago by
Biostar
20 • written 7.7 years ago by
niutster
▴ 110
4
votes
8
replies
9.3k
views
Quantile normalizing prior to or after TPM scaling?
RNAseq
normalization
updated 14 months ago by
Kevin Blighe
87k • written 6.4 years ago by
mforde84
★ 1.4k
5
votes
12
replies
9.3k
views
ADMIXTURE: "Invalid chromosome code. Use integers!"
admixture
genome
7.2 years ago by
beneficii
▴ 60
7
votes
8
replies
9.3k
views
Removing rRNA and tRNA sequences using GTF files
RNA-Seq
7.7 years ago by
pixie@bioinfo
★ 1.5k
4
votes
1
reply
9.2k
views
Need help with heatmaps in R, how to draw select genes or selected pathway??
RNA-Seq
DESEQ2
R
heatmap
ontology
updated 7.6 years ago by
Biostar
20 • written 7.6 years ago by
marina.kimyr
▴ 20
3
votes
8
replies
9.2k
views
DiffBind: Error in `.rowNamesDF<-`(x, value = value) : invalid 'row.names' length
R
DiffBind
ChIP-Seq
5.1 years ago by
msimmer92
▴ 300
1
vote
2
replies
9.1k
views
Problem in merging 1000G and cases in Plink
merge
duplicate snp
plink
triallelic
1000G
7.6 years ago by
fatima
▴ 20
10
votes
11
replies
9.1k
views
How to adjust my manhattan plot to look better?
qqman
manhattan
R
updated 22 months ago by
Ram
43k • written 9.1 years ago by
SheelS
▴ 40
3
votes
10
replies
9.0k
views
How to remove outliers using PCA in R?
PCA
R
4.7 years ago by
zhaoliang0302
▴ 50
3
votes
4
replies
9.0k
views
how to filter vcf file based on sample DP? vcf tools does not work
vcf-filtering
sample DP
7.0 years ago by
Ana
▴ 200
3
votes
0
replies
9.0k
views
edgeR: how to make contrasts with makeContrasts
ngs
edgeR
makeContrasts
glm
dge
5.4 years ago by
m98
▴ 420
13
votes
13
replies
9.0k
views
How to do pca plot from .eigenval and .eigenvec files from Plink in R.
R
SNP
updated 6.1 years ago by
Devon Ryan
104k • written 6.1 years ago by
amitgourav.ghosh12
▴ 70
7
votes
8
replies
8.9k
views
Determining read count
trimmomatic
rna-seq
trinity
updated 7 months ago by
Ram
43k • written 8.0 years ago by
nikelle.petrillo
▴ 110
3
votes
4
replies
8.9k
views
Design Pcr Primers To Uniquely Identify A Bacterial Strain
bacteria
pcr
updated 10.5 years ago by
Biostar
20 • written 10.5 years ago by
Eric Normandeau
11k
4
votes
9
replies
8.9k
views
bcftools consensus command
vcf
bcftools
updated 13 months ago by
Ram
43k • written 4.2 years ago by
Begonia_pavonina
▴ 150
2
votes
3
replies
8.8k
views
what is the detailed information of .amb .ann .bwt .pac .sa files generated by the BWA aligner?
alignment
BWA
.ann
.bwt
.sa
updated 6.2 years ago by
WouterDeCoster
47k • written 6.2 years ago by
lffu_0032
▴ 90
5
votes
10
replies
8.8k
views
GWAS - approximate odds ratio and standard error
GWAS
imputation
updated 6.5 years ago by
Kevin Blighe
87k • written 6.5 years ago by
alessandrotestori7
▴ 420
2
votes
8
replies
8.8k
views
Questions: how to do GSEA for single cells?
RNA-Seq
3.9 years ago by
yingnanlei0202
▴ 20
0
votes
4
replies
8.8k
views
ITCN 1.6 ImageJ Plugin
software error
updated 6.4 years ago by
Biostar
20 • written 7.5 years ago by
verma
▴ 30
1
vote
3
replies
8.8k
views
Htseq Count Finding No Feature
htseq
bacteria
gene-expression
11.0 years ago by
joaslucas
▴ 90
2
votes
2
replies
8.8k
views
Plot minor allele frequency distribution in R?
gwas
maf
R
7.9 years ago by
dam4l
▴ 200
1
vote
2
replies
8.7k
views
Install Plink V1.07 on Mac
software error
7.7 years ago by
xaviera417
• 0
3
votes
13
replies
8.7k
views
Actually meaning of log2FoldChange, p-value & padj in DESeq2 results
RNA-Seq
DESeq2
differentially expressed genes
5.5 years ago by
hffqyd
▴ 10
1,000 results • Page
3 of 20
Recent Votes
Comment: Filtration Of Reads With Length Lower Than 30 From Bam
How to compare the quality of assemblies
Filtration Of Reads With Length Lower Than 30 From Bam
Answer: Filtration Of Reads With Length Lower Than 30 From Bam
Answer: How to compare the quality of assemblies
Comment: How to compare the quality of assemblies
Bedtools merge but only if intersection exists
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Comment: Free/open source 23andme-like analysis
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54k
Noted that 'accurate' wasn't amongst your criteria ;) Anyway, most variant callers are free open-source software. However, for ancestry a…
Answer: Mapping cDNA sequence of a single gene to a genome not hosted at UCSC server (wi
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> server so I cannot use Blat for this purpose. blat is avilable as a standane tool: http://hgdownload.soe.ucsc.edu/admin/exe/linux.x86…
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My favourite for this task would be [GMAP]( http://research-pub.gene.com/gmap ), which can produce GFF format with option `-f 2`. It is…
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thanks! This saved me quite some time, I was about to write code to calculate the aligned length from the CIGAR. But this can be done with …
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will look into that. Thank you very much
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Thanks..... But I want to do imputation, so I have to make it as a vcf file, but the site only has a fatsa file....
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Hi there, I let a developer know of this thread and they said they can check it out next week. Feel free to post to the https://github.com/…
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Thanks for your guide!
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I'd try those OP @samuel recommends My guess is you're new to ONT, fast5 is the 'raw data' which is current over time...other than generat…
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No. Find a tutorial, try it, then if you have specific questions, ask of the galaxy help site.
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swbarnes2
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Shouldn't you use PicardTools for this?
Comment: Downloaded pdb's on rcsb.org
by
Ram
43k
Sure. Or, one could do: bash try.bash "Homo sapiens" AHR | xargs -I v_pdb curl -s -o v_pdb.pdb https://files.rcsb.org/view/v_pdb.pdb
Comment: Downloaded pdb's on rcsb.org
by
iamsmor
• 0
thank you so much
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