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1,000 results • Page
2 of 20
Sort: Votes
Rank
Views
Votes
Replies
6
votes
5
replies
733
views
Tests for the linear and non-linear relationship between two genes
ode
drc
correlation
regression
rnaseq
updated 4 months ago by
ATpoint
82k • written 4 months ago by
cwwong13
▴ 40
6
votes
6
replies
3.2k
views
ChIP-Seq Intensity Analysis
R
ChIP-Seq
updated 11 months ago by
Ram
43k • written 6.5 years ago by
solveforj
▴ 20
6
votes
7
replies
1.7k
views
Bioinformatics Master Project With More Focus on Developing Algorithm and Software
Masters
Algorithm
Software
updated 12 months ago by
Ram
43k • written 6.9 years ago by
nilo
▴ 90
5
votes
10
replies
1.3k
views
the distribution of log2Fc and t value are not similar for bulk RNA-seq
decoupleR
RNA-seq
8 months ago by
alwayshope
▴ 40
5
votes
5
replies
266
views
Error in dimnames(x) <- dn : length of 'dimnames' [2] not equal to array extent
EGSEA
2 days ago by
Chris
▴ 280
5
votes
7
replies
2.7k
views
DESeq2 for differential gene expression on GTEx dataset
differential-gene-expression
RNA-Seq
GTex
DESeq2
updated 4 weeks ago by
Ram
43k • written 6.5 years ago by
vikram
▴ 10
5
votes
19
replies
4.0k
views
8 follow
Hisat2 aligner problem
RNA-Seq
ChIP-Seq
alignment
Assembly
software error
updated 4 months ago by
ATpoint
82k • written 5.0 years ago by
ta_awwad
▴ 340
5
votes
11
replies
1.0k
views
Make heatmap for RNA-seq with non replicate
RNA-seq
updated 9 months ago by
Ram
43k • written 9 months ago by
Chris
▴ 280
5
votes
7
replies
856
views
About the value in bigwig file
ATAC-seq
updated 10 months ago by
rfran010
▴ 900 • written 10 months ago by
Chris
▴ 280
5
votes
5
replies
7.3k
views
Converting scRNA-Seq to Bulk-RNASeq
scRNASeq
bulk-RNASeq
RNA-Seq
single-cell
updated 29 days ago by
veldahan86
• 0 • written 3.8 years ago by
Assa Yeroslaviz
★ 1.8k
5
votes
5
replies
2.5k
views
Quickly retrieve reference genome sequence within python
sequence
python
updated 6 months ago by
Feng Tian
▴ 20 • written 5.6 years ago by
gewa
▴ 20
5
votes
35
replies
3.7k
views
Reduce set of chromosomes in Pangenome graph
pangenome
vg
updated 10 months ago by
Jordan M Eizenga
▴ 460 • written 10 months ago by
anivlete
• 0
5
votes
3
replies
633
views
Strand bias in supplementary alignments from Nanopore
minimap2
nanopore
strand
updated 6 months ago by
cmdcolin
★ 3.8k • written 6 months ago by
dariober
14k
5
votes
6
replies
1.4k
views
DESeqDataSetFromHTSeqCount function taking long time and utilizing more RAM
DESeq2
R
RNA-Seq
updated 10 months ago by
Ram
43k • written 4.0 years ago by
Ranan Jyoti Sarma
▴ 90
5
votes
7
replies
969
views
Salmon index not progressing
salmon
updated 7 months ago by
Michael
54k • written 7 months ago by
camillab.
▴ 160
5
votes
5
replies
663
views
Normalization and Genome-Wide Comparisons with Chipseq
chip-seq
Chipseq
Normalization
updated 4 months ago by
Ankit
▴ 500 • written 4 months ago by
zbeddingfield3
▴ 10
5
votes
8
replies
2.0k
views
looking for tools to detect RNA contamination in DNA
RNA-Seq
DNA-Seq
contamination
QC
updated 6 months ago by
Jingjingzhang
• 0 • written 3.7 years ago by
from the mountains
▴ 230
5
votes
5
replies
1.8k
views
bio-newbie / gene research / tools and methods
methods
research
gene
updated 11 months ago by
Ram
43k • written 6.3 years ago by
wizofe
• 0
5
votes
3
replies
1.0k
views
abyss-pe genome assembly
konnector
abyss-pe
updated 10 months ago by
Ram
43k • written 5.3 years ago by
Igor Lalin
• 0
5
votes
8
replies
3.7k
views
Many Differentially expressed genes but few GO terms
differential-gene-expression
RNA-seq
gene-ontology
updated 4 weeks ago by
Ram
43k • written 6.5 years ago by
firestar
★ 1.6k
5
votes
5
replies
646
views
Counting 705 fasta header characters ('>') in human genome
human-genome
genetics
updated 6 months ago by
ATpoint
82k • written 6 months ago by
10mz1
▴ 10
5
votes
5
replies
540
views
Example MAF Files
MAF
updated 4 months ago by
Ram
43k • written 4 months ago by
anasjamshed
▴ 120
5
votes
4
replies
1.7k
views
Detection of DE genes among different tissues of an organism during time - RNA seq
detection
DE-genes
multi-treatments
time-series
updated 11 months ago by
Ram
43k • written 7.8 years ago by
statfa
▴ 760
5
votes
6
replies
1.7k
views
Filter out Bam not overlapping with Bed File (keeping a read and its mate)?
samtools
bam
bed
updated 10 months ago by
Ram
43k • written 18 months ago by
Eliveri
▴ 350
5
votes
6
replies
834
views
Calculate the percentage of genomic region covered from the BED file.
NGS
sequencing
genomics
exome
genes
updated 9 months ago by
rfran010
▴ 900 • written 9 months ago by
adarsh_pp
▴ 40
5
votes
8
replies
1.0k
views
sc-RNA seq pipeline
scRNA-seq
NGS
RNA-Seq
4 months ago by
Researcher
▴ 30
5
votes
6
replies
439
views
7 follow
Seeking Help with Unexpected MA Plot Output
MAplot
RNAseq
Rstudio
updated 5 weeks ago by
Istvan Albert
100k • written 5 weeks ago by
Pumla
• 0
5
votes
1
reply
696
views
Challenges in Variant Calling and Genotyping with Short-Read Data Mapped to a Pangenome Graph: Seeking Guidance
vg
pggb
giraffe
updated 6 months ago by
Jordan M Eizenga
▴ 460 • written 6 months ago by
Kyran
▴ 30
5
votes
7
replies
970
views
Are datasets for a unique cells, that downloded using sratoolkit?
RNA-Seq
sequencing
updated 11 months ago by
supernovamik
• 0 • written 4.4 years ago by
ee.mohseni.alert
▴ 50
5
votes
2
replies
938
views
Recommended way to normalize SmartSeq2 gene expression matrix to better match 10X expression data
rna-seq
smartseq2
r
updated 6 months ago by
yhdist
▴ 70 • written 7 months ago by
Cookin
▴ 10
5
votes
8
replies
2.5k
views
SV calling using giraffe/vg
vg
Giraffe
calling
structural
variant
updated 9 months ago by
Jordan M Eizenga
▴ 460 • written 16 months ago by
TN
• 0
5
votes
11
replies
1.4k
views
Interpret IGV output inversion
variant-calling
IGV
alignment
updated 9 months ago by
cmdcolin
★ 3.8k • written 9 months ago by
pablo
▴ 300
5
votes
4
replies
718
views
FASTQ to BAM to CRAM to FASTQ
Samtools
6 months ago by
ManuelDB
▴ 80
5
votes
10
replies
878
views
Error when viewing a bam file
samtools
updated 10 months ago by
Ram
43k • written 12 months ago by
Chris
▴ 280
5
votes
3
replies
401
views
samtools view: error reading file
samtools
bowtie2
updated 9 weeks ago by
bioinfo_ga
▴ 70 • written 9 weeks ago by
ray
• 0
5
votes
8
replies
2.0k
views
snpeff install error
snpeff
updated 12 months ago by
Ram
43k • written 12 months ago by
bestone
▴ 30
5
votes
7
replies
1.5k
views
error while using cyvcf2 to parse the vcf file
cyvcf2
vcf
htslib
updated 12 months ago by
Ram
43k • written 23 months ago by
rheab1230
▴ 140
5
votes
1
reply
688
views
Learning Linux advance commands
grep
awk
linux
sed
updated 7 months ago by
Zhitian Wu
▴ 60 • written 18 months ago by
rheab1230
▴ 140
5
votes
2
replies
1.8k
views
Batch effects from sequencing samples accross multiple flow cells.
rna-seq
batch
batch-effect
sequencing
updated 23 days ago by
Ram
43k • written 3.0 years ago by
Mat
▴ 60
5
votes
3
replies
553
views
Visualisation of accessible regions in single cell atacseq data
visualization
scATAC-seq
single-cell
updated 7 months ago by
Ram
43k • written 7 months ago by
sarahmanderni
▴ 100
5
votes
5
replies
587
views
Generate BED file
bed
3 months ago by
daffodil
▴ 10
5
votes
8
replies
633
views
Multiple threads on ubuntu server
Ubuntu
updated 3 months ago by
colindaven
6.4k • written 3 months ago by
oghzzang
▴ 50
5
votes
7
replies
3.2k
views
8 follow
bwa mem -T (alignment score) not doing anything
SNP
genome
sequence
updated 6 months ago by
Istvan Albert
100k • written 5.9 years ago by
chris.bird
▴ 10
5
votes
4
replies
1.2k
views
Converting Bam file to Fasta (Zipped)
bedtools
samtools
updated 10 months ago by
Ram
43k • written 18 months ago by
Eliveri
▴ 350
5
votes
1
reply
635
views
Enricher with Gene Symbols
DGE
ClusterProfiler
Enrich
ORA
updated 8 months ago by
bk11
★ 2.4k • written 8 months ago by
Manuel Sokolov Ravasqueira
▴ 100
4
votes
6
replies
2.1k
views
Single nucleotide Polymorphism (SNP)
SNP
updated 10 months ago by
Ram
43k • written 9.1 years ago by
Harish Sanja
▴ 10
4
votes
11
replies
1.7k
views
Check Strandedness
Check_Strandedness
how_are_we_stranded_here
leafcutter
bash
updated 6 months ago by
Brian Bushnell
20k • written 8 months ago by
Y
• 0
4
votes
1
reply
642
views
How to interpret Clustree results?
scRNA
clustering
clustree
updated 8 months ago by
LChart
3.9k • written 8 months ago by
leranwangcs
▴ 120
4
votes
3
replies
609
views
Identifying enhancers that regulate certain genes
enhancers
updated 9 months ago by
rfran010
▴ 900 • written 10 months ago by
Rozita
▴ 40
4
votes
8
replies
1.8k
views
Error while running nf-core/rnaseq pipeline
nf-core
RNA-seq
11 months ago by
eesha28112001
• 0
1,000 results • Page
2 of 20
Recent Votes
Comment: Question about methylation location
Comment: Question about methylation location
Comment: Question about methylation location
How to use minimap2?
Comment: RNA seq analysis
Comment: Filtering Multi-sample VCF file for all except one Genotype
Truncated metadata file report from ENA Portal API
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★ 1.9k
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Recent Replies
Comment: cellranger error message
by
Max
• 0
I think the problem is your fastq_id. This should also read "RabhiN_PHLGEX". Hope this helps!
Comment: How to format "I" and "D" in vcf version 4.2 for liftover analysis in GATK
by
Giulio Genovese
▴ 390
@yokofakun is correct. Also, do notice that the GATK option `--RECOVER_SWAPPED_REF_ALT True` does not work with indels. In general, if your…
Comment: How to format "I" and "D" in vcf version 4.2 for liftover analysis in GATK
by
Pierre Lindenbaum
161k
> Don't forget to follow up on your threads. If an answer was helpful, you should upvote it; if the answer resolved your question, you shou…
Comment: How to format "I" and "D" in vcf version 4.2 for liftover analysis in GATK
by
Pierre Lindenbaum
161k
I think this is useless, in the gatk doc: > For each variant, the tool will look for the target coordinate, reverse-complement and left-al…
Comment: Too many unpaired forward reads found by Trimmomatic
by
GenoMax
142k
Ideally you will know which adapters to use but if you don't then programs like `fastp` can auto-detect them. You could also use `bbduk.sh`…
Comment: UMI-Tools knee-method has great influence on the results of white list
by
i.sudbery
19k
With the `--read2-only` option (which isn't available yet on the bioconda version), this will complain about a lack of `--bc-pattern`. How…
Comment: samtools tview symbols
by
Ruqaiya
• 0
What does the star mean then ?
Comment: RNA seq analysis
by
prifa
▴ 10
it's raw data **fastq.gz**, so for example I have 4 different samples from different tissue, sample A with 3 replicates, samples B,C and D …
Answer: Filtering Multi-sample VCF file for all except one Genotype
by
Pierre Lindenbaum
161k
> The goal is to remove all the variants which are unique to the KWSBambina sample. using jvarkit vcffilterjdk https://jvarkit.readthedo…
Comment: Too many unpaired forward reads found by Trimmomatic
by
SilhouetteQ
• 0
The first example used the adapter file NexteraPE-PE.fa, but it generated more than 50% unpaired data...... The content of NexteraPE-PE.fa…
Comment: Filtering Multi-sample VCF file for all except one Genotype
by
schmince
• 0
Ok so I definitely didn't understand at first what my goal was. The goal is to remove all the variants which are unique to the KWSBambina…
Comment: Question about methylation location
by
dthorbur
★ 1.9k
What data do you have? Generally, you start with sequencing data, which you need to clean and then map to a reference genome. Then dependin…
Comment: Too many unpaired forward reads found by Trimmomatic
by
GenoMax
142k
> when I didn't provide the adapter file Still see the file here `ILLUMINACLIP:./NexteraPE-PE.fa:2:30:10 `, unless that is an empty file.
Comment: Too many unpaired forward reads found by Trimmomatic
by
SilhouetteQ
• 0
Interestingly, when I didn't provide the adapter file, the number of unpaired forward reads was significantly reduced: TrimmomaticPE…
Comment: Alignment of samples with spike-in
by
GenoMax
142k
> but then if you only allow to map uniquely mapped reads, you are losing spike-in information, How so? Spike-in's are generally unique s…
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