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1,000 results • Page
2 of 20
Sort: Views
Rank
Views
Votes
Replies
1
vote
13
replies
12k
views
"[E::bgzf_read] Read block operation failed" error - possible truncation/corruption of BAM file
samtools
updated 2.3 years ago by
darklings
▴ 520 • written 4.0 years ago by
gordo2b
• 0
0
votes
1
reply
12k
views
PLINK 1.9 - Converting PED/MAP to BED/BIM/FAM with missing values
plink
updated 7.2 years ago by
Biostar
20 • written 7.2 years ago by
rednalf
▴ 90
0
votes
3
replies
12k
views
edgeR: likelihood ratio test or quasi-likelihood F-test?
R
rna-seq
next-gen
6.5 years ago by
moxu
▴ 510
2
votes
13
replies
12k
views
8 follow
(ERR): bowtie2-align exited with value 1
software error
RNA-Seq
updated 5.7 years ago by
basucsmcri
• 0 • written 6.6 years ago by
biostarsb
▴ 30
3
votes
2
replies
12k
views
ExAC PLI score calculation
DNA-Seq
6.6 years ago by
jonessara770
▴ 240
4
votes
9
replies
12k
views
Seqtk subseq: structure of file name.lst
sequence
next-gen
updated 5.4 years ago by
Ram
40k • written 5.4 years ago by
ste.lu
▴ 80
0
votes
3
replies
11k
views
Extracting Specific Columns from Multiple Files & Writing to File Python
python
file-handeling
7.4 years ago by
BioICoder
▴ 40
7
votes
9
replies
11k
views
Different alignment rates for Hisat2 and STAR, Hisat2 has lower alignment rate and STAR have many multi aligned reads
RNA-Seq
updated 6.0 years ago by
Satyajeet Khare
★ 1.6k • written 6.0 years ago by
SMILE
▴ 170
8
votes
5
replies
11k
views
samtools tview symbols
samtools
updated 10 months ago by
Ram
40k • written 8.2 years ago by
biolab
★ 1.4k
1
vote
13
replies
11k
views
MarkDuplicates memory issue
alignment
Picard
MarkDuplicates
7.7 years ago by
cacampbell
▴ 50
3
votes
8
replies
11k
views
6 follow
How do I go from UniProt ID to retrieving the gene name?
sequence
5.9 years ago by
a.rex
▴ 350
0
votes
4
replies
11k
views
Convert .gbf file to .gbk or .gff
gbk
gff
gbf
updated 8 months ago by
Ram
40k • written 8.4 years ago by
che.bellaj
• 0
4
votes
7
replies
11k
views
Grab Coordinate Of Centromeres From Ucsc
ucsc
10.4 years ago by
jeansimon32
▴ 170
2
votes
3
replies
11k
views
converting maf to vcf
Exome
maf2vcf
updated 8 months ago by
Ram
40k • written 8.4 years ago by
ashishchahl
• 0
3
votes
4
replies
11k
views
Zlib.Error: -3 While Decompressing: Invalid Distance To Far Back (By Using Macs For Chip-Seq Data)
error
12.0 years ago by
Lisanne
• 0
13
votes
6
replies
11k
views
6 follow
MAF vs VAF
sequencing
5.5 years ago by
lauren.wahyudi
▴ 40
41
votes
55
replies
11k
views
6 follow
hash function for DNA sequences
hash
hashing
DNA
7.5 years ago by
midox
▴ 290
1
vote
2
replies
11k
views
Downloading BAM files GEO/SRA
bam
sra
geo
samtools
sratoolkit
7.2 years ago by
ilobelo
▴ 10
6
votes
7
replies
11k
views
bedtools intersect bed and vcf, coordinates problem
bedtools
bed
vcf
6.5 years ago by
abascalfederico
★ 1.2k
2
votes
4
replies
11k
views
Pymol-Generate Pymol Movie To Mpeg
pymol
updated 20 months ago by
Ram
40k • written 11.7 years ago by
Reyhaneh
▴ 530
3
votes
16
replies
11k
views
combining z-scores into a single z-score value
excel
R
statistics
updated 3 months ago by
Ram
40k • written 4.5 years ago by
Star
▴ 60
2
votes
8
replies
11k
views
Loading Custom Genome In Igv Is Not Displaying Genes, Names Match.
igv
gff
reference
contigs
11.6 years ago by
Nickengland
▴ 130
4
votes
14
replies
10k
views
All the reads aligned using STAR have low mapping quality (0-3). What is happening?
mapping quality
STAR
BWA
alignment
7.2 years ago by
kirannbishwa01
★ 1.6k
3
votes
4
replies
10k
views
basename: missing operand
snp
4.2 years ago by
evelyn
▴ 220
2
votes
0
replies
10k
views
How to plot UniFrac PCoA with 95% confidence Elipses in R
metagenomics
ordiellipse
vegan
R
phyloseq
updated 18 months ago by
Ram
40k • written 8.7 years ago by
c.v.oflynn
▴ 100
3
votes
1
reply
10k
views
Negative P-Values
gene
genome
next-gen-sequencing
updated 13 months ago by
Ram
40k • written 8.1 years ago by
stevenlang123
▴ 200
7
votes
8
replies
10k
views
Picard tools duplicate removal
RNA-Seq
picard-tools
6.0 years ago by
blur
▴ 280
2
votes
1
reply
10k
views
Calculate Linkage Disequilibrium For Snps (Using R^2)
snp
linkage
10.2 years ago by
TitoPullo
▴ 180
3
votes
2
replies
10k
views
BWA-MEM Vs BWA-ALN
next-gen
genome
alignment
7.4 years ago by
SOHAIL
▴ 400
11
votes
10
replies
10k
views
Extracting from tophat outputs reads pairs and splice-junctions with a single best match
TOPHAT
RNA-Seq
updated 21 months ago by
Ram
40k • written 9.1 years ago by
trakhtenberg
▴ 160
0
votes
1
reply
10k
views
Is it normal that nearly all of p-value is equal to 0.1 in PERMANOVA analysis
PERMANOVA
statistics
metagenomics
updated 2.8 years ago by
dqq102829
• 0 • written 3.7 years ago by
zhangdengwei
▴ 210
1
vote
2
replies
10.0k
views
Converting MSTRG from stringtie with gene name
RNA-Seq
Stringtie
updated 5.7 years ago by
Biostar
20 • written 5.7 years ago by
fhassanz
▴ 20
3
votes
9
replies
10.0k
views
Error with samtools faidx...Different line length in sequence
samtools
faidx
updated 5.4 years ago by
Biostar
20 • written 5.5 years ago by
oars
▴ 190
0
votes
0
replies
10.0k
views
Map Between Uniprot Accesion And Gene.Symbol Using R Or/And Mysql
r
bioconductor
mysql
9.7 years ago by
jfertaj
▴ 110
2
votes
2
replies
9.9k
views
How to make clusters in heat map using ggplot2?
RNA-Seq
rna-seq
R
4.4 years ago by
John
▴ 270
1
vote
1
reply
9.9k
views
Raxml bootstrap support values
figtree
raxml
bootstrap
updated 24 months ago by
Ram
40k • written 9.4 years ago by
JackBel
• 0
3
votes
6
replies
9.9k
views
6 follow
How to calculate genetic correlation with R
R
updated 16 months ago by
ibomsolomon
• 0 • written 9.4 years ago by
Tohamy
▴ 80
7
votes
9
replies
9.8k
views
Samtools Index Segmentation Fault
samtools
index
9.5 years ago by
Noushin N
▴ 600
0
votes
0
replies
9.8k
views
pheatmap row annotation and title font size questions
heatmap
pheatmap
updated 8 months ago by
Ram
40k • written 8.4 years ago by
neokao
• 0
1
vote
5
replies
9.8k
views
What Agilent Interval Files (.Bed) Should I Use For Exome Variant Calling With Gatk?
bed
agilent
gatk
updated 3.6 years ago by
Karma
▴ 310 • written 9.8 years ago by
newDNASeqer
▴ 750
2
votes
16
replies
9.7k
views
Tophat with Bowtie2 long index
tophat
bowtie
updated 20 months ago by
Ram
40k • written 9.2 years ago by
BDK_compbio
▴ 140
13
votes
22
replies
9.7k
views
SVA : Setting up the data from an ExpressionSet and applying sva function to extimate batches
sva
combat
batch effects
updated 6.0 years ago by
Biostar
20 • written 6.2 years ago by
lessismore
★ 1.3k
2
votes
8
replies
9.6k
views
Size of typical genomic data
genomic
updated 6 months ago by
Ram
40k • written 5.4 years ago by
Nicolas Rosewick
10k
3
votes
10
replies
9.5k
views
How can I obtain SNP from TCGA?
Risky-allele
BRCA
SNP
updated 20 months ago by
Ram
40k • written 9.0 years ago by
purmod
▴ 10
3
votes
3
replies
9.4k
views
bcftools mpileup output format
bcftools
mpileup
5.1 years ago by
tarek.mohamed
▴ 350
3
votes
4
replies
9.4k
views
Aligning RNA seq data to genome or transcriptome
RNA-Seq
ngs
transcriptome
genome
updated 6.0 years ago by
Ram
40k • written 6.0 years ago by
KVC_bioinfo
▴ 590
6
votes
3
replies
9.4k
views
Sequence duplication levels-RNA Seq
RNA-Seq
updated 3.0 years ago by
joshua.theisen
▴ 30 • written 5.5 years ago by
makwana.kd
▴ 50
0
votes
2
replies
9.4k
views
DESeq2 pheatmap returns Error in check.length("fill") : 'gpar' element 'fill' must not be length 0
RNA-Seq
DESeq2
gpar
pheatmap
5.9 years ago by
Anthony.Knox
▴ 60
0
votes
8
replies
9.4k
views
how to find a read by name in a bam file
next-gen-sequencing
updated 3 months ago by
Ram
40k • written 6.2 years ago by
himanimalhotra89
• 0
5
votes
8
replies
9.3k
views
7 follow
Converting SNP names from Illumina GSA array to rsID using PLINK
SNP
plink
6.0 years ago by
dam4l
▴ 190
1,000 results • Page
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Recent Votes
Answer: Low Alignment rate
Comment: Filtering VCF to divide with equal sizes
Answer: How to plot proportion of cells in each cluster with scanpy?
Comment: How the first sequencing product removed in pair end sequencing
Comment: WGCNA Labeled Heatmap
C: Can I manually add nCount_RNA & nFeature_RNA to a converted Seurat object?
Comment: Hisat2 index and alignment question
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Comment: Low Alignment rate
by
Mehwish
• 0
Thanks alot! This worked out for me https://ftp.ensembl.org/pub/release-110/fasta/homo_sapiens/dna/Homo_sapiens.GRCh38.dna.toplevel.fa.gz …
Comment: Violin plot (Monocle 3) - Troubleshooting
by
Ram
40k
The error message tells me there is the possibility of a conflicting function called `plot_genes_violin` that accepts one parameter and err…
Comment: Violin plot (Monocle 3) - Troubleshooting
by
bk11
★ 1.2k
I m not sure why you have problem there. I do not encounter any problem. May be your gene list are not present in your source object. Pleas…
Comment: Violin plot (Monocle 3) - Troubleshooting
by
Ram
40k
What is the output to: ```r help.search('plot_genes_violin', agrep=FALSE, ignore.case=FALSE, fields=c('name')) lsf.str() sessionInfo() ```
Comment: Violin plot (Monocle 3) - Troubleshooting
by
seattlescientist_01
• 0
I see the error message but I'm confused on what it's telling me.
Answer: Bacterial Pangenome Analysis
by
liorglic
★ 1.2k
I am not sure I understand why you think there is a problem with your analysis. It makes perfect sense that different blastp cutoffs produc…
Comment: How to plot proportion of cells in each cluster with scanpy?
by
bioinfo
▴ 110
Thank you for replying again. The "type" still causes issues but the reply by Radu Tanasa worked.
Comment: How to plot proportion of cells in each cluster with scanpy?
by
bioinfo
▴ 110
Thank you so much. That worked perfectly and it was much faster than what I was trying.
Answer: How to plot proportion of cells in each cluster with scanpy?
by
Radu Tanasa
▴ 60
Hi. If I get this right, you simply need to compute the percentage of cells in each cluster at the dataset level? ```py import pandas as p…
Comment: Should I Learn Docker to Run Command Line Bioinformatics Tool?
by
ATpoint
76k
Why would that be an advantage?
Comment: How to plot proportion of cells in each cluster with scanpy?
by
bk11
★ 1.2k
The following code will write percentage in your stacked barplot. cross_tab = pd.crosstab(adata.obs['leiden_0.6'],adata.obs['typ…
Comment: How to check RNAseq support for annotated genes?
by
BioinfoBee
• 0
@juke34 Thanks for the suggestion. I wonder if bedtool coverage or intersect can be used to check the transcript support or coverage for ea…
Comment: How to plot proportion of cells in each cluster with scanpy?
by
bioinfo
▴ 110
Because that was the code from the link. It is how they specified they had 2 groups of samples but I don't have 2 groups. Sorry for the con…
Comment: Violin plot (Monocle 3) - Troubleshooting
by
bk11
★ 1.2k
No there is no bug in this. Please see carefully what the `error` message tells to you.
Comment: How to check RNAseq support for annotated genes?
by
BioinfoBee
• 0
@michaeld Thanks. I tried it using STAR to map the transcript to the annotation gtf file, and was planning to use featureCounts/gene Counts…
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