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121,904 results • Page
676 of 2439
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Votes
Replies
1
vote
0
replies
785
views
how to tell the OR or BETA in the OR.or.BETA column in GWAS summary statistics from GWAS catalog?
gwassummary
gwascatalog
4.4 years ago by
zhoufeng2ye
▴ 10
0
votes
3
replies
1.6k
views
Multiple motif [available in .txt file ] search from large fasta file to find motif frequency then print fasta sequences
motif
fasta
frequency
4.4 years ago by
Swarna Kanchan
▴ 10
2
votes
2
replies
1.3k
views
how to have aligned region in fasta format using blastn?
blastn
fasta
updated 4.3 years ago by
Ram
45k • written 4.4 years ago by
mthm
▴ 80
0
votes
4
replies
2.4k
views
Help with salmon quantification of samples with de novo transcriptome
salmon
denovo
tximport
updated 4.4 years ago by
ponganta
▴ 590 • written 4.5 years ago by
codyas
• 0
2
votes
0
replies
961
views
what are the parameters we should change when we run VariantsToTable of GATK in splitting multi allelic mode?
variantstotable
gatk
vcf
picard
4.4 years ago by
DareDevil
★ 4.4k
0
votes
0
replies
416
views
fetching first column as a class attribute in arulesCBA
arulesCBA
R
4.4 years ago by
hebasamysaeid1
• 0
1
vote
4
replies
2.2k
views
MA plots with similar distribution but display difference in significantly expressed genes
reads
MAplot
DEG
rna
DESeq2
updated 4.4 years ago by
seidel
11k • written 4.4 years ago by
fufor94
▴ 10
1
vote
1
reply
1.3k
views
PCA plot making
VCF
PCA
vcftools
SNP
updated 4.4 years ago by
prasundutta87
▴ 720 • written 4.4 years ago by
yb87625
• 0
1
vote
0
replies
1.1k
views
Could it be risky to analyse cells that are negative after cell hashing on single cell RNA sequencing?
RNA-Seq
singlecell
R
Seurat
4.4 years ago by
charlesgwellem
▴ 10
0
votes
0
replies
993
views
CNVkit flat reference file creation
CNV
ces
Flatreference
CNVkit
wes
4.4 years ago by
enes
▴ 40
10
votes
4
replies
9.0k
views
What is gnomAD allele frequency
AF
gnomAD
updated 20 months ago by
Lhl
▴ 760 • written 4.5 years ago by
Eric Wang
▴ 70
2
votes
3
replies
2.1k
views
Remove reads from bam file that partially covers a region
indel
filter
bam
4.4 years ago by
arbarharw
• 0
0
votes
3
replies
1.1k
views
Trim alignment from .sam file based on a specific tab-delimiter .bed file
sam
updated 4.4 years ago by
Pierre Lindenbaum
166k • written 4.5 years ago by
khanhlpbao
• 0
0
votes
0
replies
732
views
SNP Mapping/Characterisation and Patches
GRCh38
prioritisation
patches
SNP
4.5 years ago by
KBMP
• 0
0
votes
2
replies
1.2k
views
Help with statistic model
online
education
R
updated 4.5 years ago by
Kevin Blighe
89k • written 4.5 years ago by
Bioman
• 0
1
vote
2
replies
2.4k
views
Convert multiple rows value retrieved from ensemble biomart to comma separated list for a common ensemble gene ID.
ensembl
Biomart
R
geneontology
updated 4.2 years ago by
Ram
45k • written 4.5 years ago by
sontiroy
• 0
0
votes
0
replies
949
views
UCSC parameters for converting between human genome builds
genomics
bed
ucsc
genotyping
4.5 years ago by
jon.klonowski
▴ 210
5
votes
3
replies
1.8k
views
RNA-SEQ count data as input for Machine Learning
machine
learning
rnaseq
normalize
updated 4.5 years ago by
Dunois
★ 2.9k • written 4.5 years ago by
Alberto
• 0
2
votes
5
replies
1.9k
views
Extracting only tumor samples from Single cell RNASeq
tumor
cell
singel
RNA
updated 4.4 years ago by
jared.andrews07
★ 19k • written 4.5 years ago by
David_emir
▴ 500
9
votes
6
replies
2.1k
views
6 follow
What are some areas where machine learning is applicable in biology and cancer?
software
deep learning
updated 4.4 years ago by
krysgourlia
▴ 30 • written 5.7 years ago by
isaacbruth1234
• 0
6
votes
11
replies
2.8k
views
How are transcriptome annotations published?
RNAseq
annotation
publish
transcriptome
4.1 years ago by
Dunois
★ 2.9k
0
votes
2
replies
1.0k
views
Hetero-dimerization analysis with two FASTA files
sequence
FASTA
python
awk
bash
updated 4.4 years ago by
Ram
45k • written 4.5 years ago by
Apex92
▴ 320
3
votes
4
replies
1.9k
views
Convert per base bedgraph to Bed format
Bedgraph
perbase
Bed
Bedtools
updated 4.5 years ago by
Alex Reynolds
36k • written 4.5 years ago by
bioyas
▴ 20
5
votes
4
replies
12k
views
Why is `send` lower than `sstart` from blast format 6 output?
blast
genomics
updated 4.5 years ago by
David
• 0 • written 5.6 years ago by
O.rka
▴ 750
0
votes
0
replies
1.2k
views
bcftools isec not producing sites.txt
bcftools
4.5 years ago by
steve
★ 3.5k
3
votes
3
replies
9.3k
views
Single Cell Experiment object to Seurat without losing rowData / colData
scrna-seq
seurat
sce
updated 4.4 years ago by
jared.andrews07
★ 19k • written 4.5 years ago by
ZheFrench
▴ 590
0
votes
0
replies
764
views
Samtools vcf file filtering
samtools
RNAseq
sequencing
4.5 years ago by
bandanaschapagain
▴ 40
0
votes
2
replies
1.1k
views
integrate two single cell datasets and use transfer learning approach using annotated cell atlas
machine-learning
scRNA-Seq
updated 22 months ago by
Ram
45k • written 4.5 years ago by
das2000sidd
▴ 30
0
votes
0
replies
581
views
[Errno 2] No such file or directory: '0-rawreads' when I run Falcon unzip with hifi data
HiFi
Falcon-unzip
4.5 years ago by
Feng
• 0
1
vote
4
replies
2.2k
views
exon.bed file for coverage
NGS
bed
coverage
bedtools
updated 2.5 years ago by
Ram
45k • written 4.5 years ago by
Sabeen
▴ 30
2
votes
21
replies
4.4k
views
How to loop on two fasta files for hetero-dimerization analysis
fasta
script
python
sequence
updated 4.5 years ago by
cpad0112
21k • written 4.5 years ago by
Apex92
▴ 320
0
votes
2
replies
1.3k
views
Suggestion for modelling transcriptomics analysis
rnaseq
wgcna
linearmodel
deseq2
updated 4.3 years ago by
Ram
45k • written 4.5 years ago by
greyman
▴ 190
2
votes
7
replies
3.2k
views
Coverage NGS reads
NGS
samtools
coverage
4.5 years ago by
Sabeen
▴ 30
4
votes
7
replies
3.2k
views
How are BWA/bowtie/etc indices built for multiple fasta entries?
index
fasta
mapping
BWA
bowtie
4.4 years ago by
maxrwjones
▴ 60
0
votes
1
reply
1.7k
views
Create a phenotype file in PLINK format
gwas
phenotype
plink
updated 4.5 years ago by
Sam
★ 4.8k • written 4.5 years ago by
simone.castellana
▴ 10
1
vote
1
reply
1.6k
views
BUSCO score goes down after adding 30% more data
racon
BUSCO
genome
canu
pilon
updated 4.5 years ago by
geneticatt
▴ 140 • written 4.5 years ago by
sorrymouse
▴ 120
5
votes
7
replies
2.9k
views
Data normalization
normalization
RNA-seq
4.5 years ago by
nolwenn
▴ 10
0
votes
0
replies
787
views
Multiple Sequence Alignment using HMM
MSA
HMM
updated 4.2 years ago by
Ram
45k • written 4.5 years ago by
anasjamshed
▴ 140
0
votes
1
reply
3.4k
views
Seurat obj conversion to Anndata not accurately creating var in a h5ad file
RNA-Seq
R
Seurat
Anndata
4.3 years ago by
akh22
▴ 120
4
votes
4
replies
1.9k
views
Where to get consensus sequences of human transposable elements
database
transposons
reference
updated 4.4 years ago by
Madelaine Gogol
5.3k • written 4.5 years ago by
WouterDeCoster
48k
2
votes
13
replies
3.7k
views
8 follow
Forum:
Recommendation required for solution of computation requirements in Genomics field
DataAnalysis
NGS
Genomics
updated 4.4 years ago by
Ram
45k • written 4.5 years ago by
hafiz.talhamalik
▴ 350
0
votes
0
replies
714
views
Can I model when 2 population separeted in the past using BEAST?
populationgenetics
beast
4.5 years ago by
harmadikemil
• 0
0
votes
0
replies
928
views
How can I add text label outside the tree in iTOL ?
iTOL
annotation
tree
label
4.5 years ago by
anran04100
• 0
4
votes
4
replies
4.8k
views
Samtools sort: too many open files error
samtools
sort
updated 4.5 years ago by
jkbonfield
★ 1.3k • written 4.5 years ago by
rekren
▴ 40
1
vote
0
replies
1.1k
views
Manta SV caller: Why is the ${MANTA_INSTALL_PATH}/bin/configManta.py.ini file missing?
Basespace
Manta
4.5 years ago by
ilante
▴ 30
0
votes
0
replies
1.2k
views
One-sided test with LDSC --h2 flag and custom annotations
heritability
ldsc
partitioned
4.5 years ago by
gokberk
▴ 90
0
votes
2
replies
2.6k
views
heterogeneity in cluster when using Seurat Doheatmap
scRNAseq
cluster
r
Seurat
seurat
4.5 years ago by
Jie
• 0
45
votes
7
replies
47k
views
9 follow
Any Good Bam And Sam Viewer?
viewer
sam
bam
updated 3.7 years ago by
Ram
45k • written 14.0 years ago by
Ken
▴ 170
7
votes
14
replies
4.1k
views
Repeat masking problem
repeatmasking
ngs
repeatmasker
4.4 years ago by
Shri hari
▴ 40
0
votes
0
replies
710
views
Resistome Analyzer Report
bwa
metagenomic
resistome
4.5 years ago by
Bio_Crap
• 0
121,904 results • Page
676 of 2439
Recent Votes
Answer: Tried building a compact sequence format with 4-bit storage
Tried building a compact sequence format with 4-bit storage
Shift in RNA 3' position, Term-Seq vs RNASeq
Comment: STARlong for pacbio Isoseq reads
Comment: Automatically annotating a feature using a genbank file
Answer: Is this PCA plot correct??
Answer: Is this PCA plot correct??
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Recent Replies
Comment: Is total miRNA in EV constant? Implications for library size normalization.
by
Gordon Smyth
★ 8.3k
RNA-seq is very good at relative analyes. It would be straightforward to determine which miRNAs are relatively more abundant, compared to o…
Comment: Tried building a compact sequence format with 4-bit storage
by
Pranava
▴ 10
Woah!!! Thank you very much, Matthias. I honestly didn't even know some of those existed and I will definitely go through them and try to u…
Answer: Tried building a compact sequence format with 4-bit storage
by
Matthias Zepper
5.1k
Hello Pranava, Thanks for sharing your repository. Devising a new file format is an interesting undertaking and certainly a task with many…
Answer: Gene Ontology Enrichment with LOC gene IDs in Common Carp (Cyprinus carpio)
by
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153k
`LOC` gene ID's are often assigned to uncharacterized genes and you may not get useful information from databases for them, thus they will …
Comment: Whole Genome Sequencing IG regions
by
GenoMax
153k
> are the calls I am seeing reliable or should I take them with something of a pinch of salt? Not sure what calls you are referring to but…
Comment: RNA-SEQ where only a subset of genes is of interest
by
piffelpaff
• 0
Sorry to revive this ancient thread but I'm currently discussing the same question with some people in my lab and would love to somebody po…
Answer: STARlong for pacbio Isoseq reads
by
YuZJ
• 0
Hello, you may try deSALT (DOI: 10.1186/s13059-019-1895-9, GitHub: ydLiu-HIT/deSALT) or uLTRA (DOI: 10.1093/bioinformatics/btab540, GitHub:…
Comment: Shift in RNA 3' position, Term-Seq vs RNASeq
by
acvill
▴ 350
Without knowing the details of the Term-seq method, could the 38 nt shift be accounted for by the difference in the position of the ribosom…
Comment: STARlong for pacbio Isoseq reads
by
Buffo
★ 2.4k
Thanks, I'll give it a try.
Comment: STARlong for pacbio Isoseq reads
by
GenoMax
153k
You could give `mapPacBio.sh` from BBMap suite a try while you wait for other answers. That works for reads up to 6 kb. BBMap has a new hom…
Comment: STARlong for pacbio Isoseq reads
by
Buffo
★ 2.4k
The average is 1.8kb. I was planning to post it on GitHub, but it seems like the repository has been unattended for the last months, so I d…
Comment: Getting just fastqc.zip file?
by
GenoMax
153k
Yes, You can either use it on command line or use the graphical user interface.
Comment: STARlong for pacbio Isoseq reads
by
GenoMax
153k
What is the average length of your reads? That error sounds like a bug, so you may want to post that on `STAR` repo as an issue. I assume …
Comment: Getting just fastqc.zip file?
by
pourhangleila95
• 0
I want to perform fastQC on my data.Do you use fastQC software for doing it?
Comment: Whole Genome Sequencing IG regions
by
719
• 0
Sorry for the poor wording of the original post, also should say I really appreciate people taking a moment to look at my post. My main con…
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