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1,000 results • Page
1 of 20
Sort: replies
Rank
Views
Votes
Replies
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
8
votes
25
replies
1.9k
views
construction of a database
sql
noSQL
neo4j
database
updated 11 days ago by
Ram
38k • written 22 months ago by
Debut
▴ 20
23
votes
22
replies
38k
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 4 months ago by
Nicole
• 0 • written 4.9 years ago by
gaelgarcia
▴ 250
5
votes
22
replies
6.4k
views
SVM for classified gene expression data
R
svm
microarray
updated 8 months ago by
Ram
38k • written 7.2 years ago by
Shaurya Jauhari
▴ 50
2
votes
22
replies
1.1k
views
6 follow
Find ~1 Mb regions of genome that are shared by two or more WGS samples?
pedigree
linkage
genetics
5 months ago by
Joel Wallenius
▴ 100
0
votes
21
replies
1.6k
views
HTSeq-Count: no_feature too high?
htseq-count
5 months ago by
sea.joson
▴ 10
9
votes
20
replies
3.2k
views
Solve SAM issues flagged by Picard's ValidateSamFile
Picard
SAM
updated 10 days ago by
Ram
38k • written 4.6 years ago by
marongiu.luigi
▴ 680
5
votes
20
replies
3.2k
views
DiscoSnp Segmentation fault
snp
discosnp
updated 6 months ago by
Ram
38k • written 7.6 years ago by
Hans
▴ 130
8
votes
20
replies
1.8k
views
Converting runpsipred Script to Work on Windows OS
psipred
windows
updated 10 months ago by
Ram
38k • written 4.7 years ago by
Bara'a
▴ 270
18
votes
19
replies
1.6k
views
6 follow
Extremely important marker gene has many reads based on IGV viewer but no quantified reads
rna-seq
sequencing
igv
alignment
next-gen
updated 4 months ago by
Ram
38k • written 4.2 years ago by
rbkh09
• 0
0
votes
19
replies
1.0k
views
scatterplot in R
microarray
expression
gene
updated 6 months ago by
Ram
38k • written 6 months ago by
bioinformatics
▴ 10
7
votes
19
replies
2.3k
views
mapping script process sleeping on server.
alignment
updated 10 months ago by
Ram
38k • written 8.1 years ago by
lvogel
▴ 30
2
votes
18
replies
1.7k
views
I need help in this
gene
weblems
alignment
updated 8 months ago by
Ram
38k • written 7.3 years ago by
efosa15
• 0
4
votes
18
replies
3.3k
views
Significance of reads mapping to Viruses - FusionCatcher
RNA-Seq
virus
reads
fusion
updated 7 months ago by
Ram
38k • written 7.3 years ago by
Joel TM
▴ 60
3
votes
18
replies
915
views
6 follow
What sequencing/alignment artifact is this?
variants
mutect
sequencing
alignment
mitochondria
5 months ago by
lacb
▴ 120
0
votes
17
replies
4.1k
views
Finding True SNPs after hard filtering on GATK
SNP
updated 6 months ago by
Ram
38k • written 7.6 years ago by
jigarnt
▴ 30
9
votes
16
replies
2.9k
views
6 follow
covert SAM to full length fasta
fasta
SAM
updated 10 days ago by
Ram
38k • written 4.6 years ago by
marongiu.luigi
▴ 680
0
votes
16
replies
3.6k
views
Count read with summarizeOverlaps result 0 for all sample
RNA-Seq
updated 9 months ago by
Ram
38k • written 8.0 years ago by
bharata1803
▴ 550
4
votes
16
replies
1.1k
views
How to extract intron counts from total RNA Sequencing?
featurecounts
RNAseq
htseq
STAR
4 months ago by
barrypraveen
▴ 110
0
votes
16
replies
1.4k
views
How to convert ncbi gff file to ensembl gff format
bcftools
gff
updated 11 days ago by
Ram
38k • written 7 months ago by
yoser4
▴ 10
7
votes
16
replies
2.0k
views
Insert size selection for RNASeq data: does it make sense?
RNA-Seq
sequencing
updated 5 days ago by
Ram
38k • written 5.5 years ago by
Matteo Schiavinato
★ 3.6k
20
votes
15
replies
25k
views
8 follow
Converting SNP from chr:pos to rs number using PLINK?
plink
SNP
updated 8 months ago by
Ram
38k • written 7.2 years ago by
dam4l
▴ 190
0
votes
15
replies
3.0k
views
Identify genes in a tophat aligned bam/sam file
blast
alignment
rna-seq
gene
updated 3 months ago by
Ram
38k • written 7.8 years ago by
gchaves
• 0
3
votes
15
replies
1.2k
views
Overlapping regions in a BED file
regions
BED
Sequence
exons
annotation
9 months ago by
Matej
• 0
6
votes
15
replies
956
views
The Best Cloud Solution For Genomics
cloud
data-sharing
genomics
workflow
updated 8 months ago by
Ram
38k • written 9 months ago by
davidmaimoun
▴ 50
1
vote
15
replies
1.2k
views
Samtools merge Illumina and PB bam file empty
Illumina
samtools
Bam
PacBio
updated 10 days ago by
Ram
38k • written 2.6 years ago by
talbots
• 0
0
votes
15
replies
1.3k
views
Chromosome accession numbers correspond to which chromosome?
bam
chromosome
bed
4 months ago by
amy__
▴ 50
10
votes
15
replies
5.2k
views
convert fasta/gb to vcf
fasta
vcf
genbank
gff
updated 10 days ago by
Ram
38k • written 4.5 years ago by
marongiu.luigi
▴ 680
2
votes
14
replies
834
views
Annotating the multi sample vcf file
vcf
annotation
3 months ago by
Peerzada
• 0
5
votes
14
replies
1.2k
views
How to Calulate Allele Frequency from a VCF File?
frequency
allele
VCF
updated 8 weeks ago by
Jeremy Leipzig
21k • written 9 weeks ago by
Emoji
• 0
1
vote
14
replies
1.4k
views
Counts all read zero after alignment?
alignment
rna-seq
updated 9 months ago by
Ram
38k • written 19 months ago by
tul66893
• 0
5
votes
14
replies
1.4k
views
Removing sequences that contain deletion mutations in them from a fasta file (with python)
python
8 months ago by
Mustafa
▴ 10
0
votes
14
replies
1.1k
views
Corrplot heatmap crunched up and unreadable
Corrplot
heatmap
10 months ago by
aropri
▴ 130
6
votes
14
replies
2.6k
views
mapping RNAseq reads to a genbank isoforme that is not in Reference Annotation
RNA-Seq
sequence
cufflinks
new isoform in rnaseq
updated 8 months ago by
Ram
38k • written 7.1 years ago by
fta.mirzadeh
• 0
0
votes
14
replies
3.2k
views
ABySS - Out of memory using 64 cores (520GB)
abyss
assembly
updated 5 months ago by
Ram
38k • written 7.6 years ago by
wjar6718
• 0
0
votes
14
replies
1.1k
views
Error using HTSEq_count
HTSeq
python
10 weeks ago by
felipead66
▴ 110
1
vote
13
replies
1.0k
views
Ete3 build - ValueError: Error parsing Phyml result
ete3
ete3toolkit
ete
phyml
build
updated 5 months ago by
Matthias Zepper
3.4k • written 5 months ago by
nitinra
▴ 50
0
votes
13
replies
663
views
Use bcftools isec to find denovo mutations
mutations
denovo
updated 5 weeks ago by
Ram
38k • written 5 weeks ago by
anasjamshed
▴ 120
6
votes
13
replies
6.0k
views
DESeq2 and edgeR - no agreement between results
RNA-Seq
edgeR
DESeq2
updated 7 months ago by
Ram
38k • written 7.3 years ago by
ilyco
▴ 60
6
votes
13
replies
658
views
Error with STAR
STAR
updated 23 days ago by
Ram
38k • written 25 days ago by
Chris
▴ 70
1
vote
13
replies
2.6k
views
Pooled / polyploid samples
discosnp
updated 6 months ago by
Ram
38k • written 7.6 years ago by
tkitapci
▴ 60
12
votes
13
replies
2.1k
views
Gene Expression and Systems Biology (homework)
gene
homework
updated 3 months ago by
Ram
38k • written 7.7 years ago by
sarathkurichiyil
• 0
1
vote
13
replies
937
views
Samtools indexing problem during bwa mem alignment
Alignment
bwa
samtools
9 months ago by
GlouGlou
• 0
1
vote
13
replies
2.4k
views
If GI number in list1 is present in genbank file, make new list and append location information
python
genbank
biopython
updated 11 months ago by
Ram
38k • written 8.1 years ago by
pawlowac
▴ 80
1
vote
13
replies
3.2k
views
Clarification on the “orientation” of chromosomal rearrangements in mate-pair or paired-end sequencing
sequencing
alignment
Assembly
updated 11 months ago by
Ram
38k • written 8.1 years ago by
alec_djinn
▴ 380
7
votes
13
replies
3.6k
views
DESeq2: can I correct for relatedness when using data from multiplex families?
DESeq2
RNA-Seq
Multiplex-families
updated 11 months ago by
Ram
38k • written 8.2 years ago by
alesssia
▴ 580
1
vote
13
replies
826
views
RNAseq for DE purpose
RNAseq
updated 8 weeks ago by
swbarnes2
13k • written 8 weeks ago by
m.habib
• 0
4
votes
13
replies
25k
views
6 follow
[main_samview] fail to read the header from sample.bam
alignment
updated 9 months ago by
Qboy
• 0 • written 5.1 years ago by
sambioinfo2018
▴ 20
8
votes
13
replies
768
views
Mapped reads not mapping to a real sequence?
bam
sam
samtools
kallisto
6 weeks ago by
txema.heredia
▴ 70
2
votes
13
replies
1.5k
views
[RNAseq, featureCounts] Can paired-end data be processed as single end?
paired-end
RNAseq
featureCounts
7 months ago by
Texx
• 0
1,000 results • Page
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Recent Votes
Answer: how can i filter a sam file from a paf file
Answer: Align miRNA library (small RNA-seq) without trimming
Answer: Snakemake workflow for trimmomatic
C: Adjust for covariates
Comment: syntax errors when running part3 all-against-all
Picard LiftOver rejecting all Variants
Comment: pyCirclize - Circular visualization in Python
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Recent Replies
Comment: how can i filter a sam file from a paf file
by
colindaven
4.6k
Just save yourself a lot of pain and learn to filter the sam/bam file efficiently. It is much more of a widespread standard than PAF.
Comment: Snakemake workflow for trimmomatic
by
GenoMax
127k
Please accept this answer (green check mark) to provide closure to this thread.
Comment: syntax errors when running part3 all-against-all
by
Sofia
• 0
When I started with the gz all-vs-all files for CHICK and ANOCA and started oma, everything ran fine, I got output. Then, in the same direc…
Comment: Quality control of Chip-seq data (NRF and PCB)
by
michelafrancesconi9
• 0
Can you explain me better? Because for the NRF I do : a) samtools view -c .bam b)samtools view -c -F 260 .bam then b/a and as a bam fi…
Comment: pyCirclize - Circular visualization in Python
by
karenkvn
▴ 40
Thank you for responding so quickly - this works perfectly!
Comment: pyCirclize - Circular visualization in Python
by
moshi
▴ 110
Please install Biopython with v1.80 or higher. If biopython>=1.80, there should be no errors.
Comment: Gene family classification using RNA-seq data
by
Dion
• 0
well, I have been given the task to retrieve gene family/categorization. I found sveral papers on family classification, but no actual pack…
Comment: pyCirclize - Circular visualization in Python
by
karenkvn
▴ 40
Thank you for this wonderful programme! I am plotting a bacterial chromosome and find that when I plot the NC_000913 chromosome using the e…
Comment: SKAT in R
by
Eliza
▴ 20
@acvill can you sujjest maybe pther tools , methods for this ? ( also for every SNP i have data how many patients had the hetro/homozygous…
Comment: TCGA-BRCA tissue and RNAseq problem
by
pinheirofabiano
▴ 10
Go to https://portal.gdc.cancer.gov > Exploration > select TCGA and the cancer type you want > select case ID to download the files and hav…
Comment: Snakemake workflow for trimmomatic
by
antoine.fauchois92
• 0
Thank you very much for your reply ! It's working now !
Comment: Dependent p values
by
Eliza
▴ 20
@lchart I'm sorry for asking another of questions but I'm new to this field , can you please explain a little more how to use SKAT , saige…
Comment: How to deal with the probe id mapping to multiple gene ids?
by
dare_devil
★ 1.7k
similar question [here][1], [here][2] and [here][3] [1]: https://support.bioconductor.org/p/54838/ [2]: https://support.bioconductor.…
Comment: How to deal with the probe id mapping to multiple gene ids?
by
dare_devil
★ 1.7k
@genomax I have used the same platform file only. If you look at probe id and their corresponding `Gene Symbol` or `ENTREZ_GENE_ID` you can…
Comment: How to deal with the probe id mapping to multiple gene ids?
by
GenoMax
127k
Where are you seeing this? [Platform file for this array][1] on GEO has these names uniquely assigned. [1]: https://www.ncbi.nlm.nih.go…
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