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121,924 results • Page
85 of 2439
Sort: Rank
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0
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4
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6 follow
Tajima's D Using SNP data ONLY
Tajima's D
SNP
updated 14 months ago by
xoaib
• 0 • written 8.4 years ago by
aberry814
▴ 80
0
votes
2
replies
6.5k
views
Calculating Tajima's D for an individual genome vs. for population of genomes vs. for genes
tajima'sD
target-of-selection
population-genetics
updated 14 months ago by
xoaib
• 0 • written 9.2 years ago by
severalorks
▴ 110
0
votes
1
reply
1.3k
views
Tajima's D calculation for specific genes in multi-sample VCF
neutrality
genetics
tajimad
updated 14 months ago by
xoaib
• 0 • written 4.2 years ago by
Muhammad
• 0
3
votes
5
replies
1.9k
views
error from msigdbr
rna-seq
msigdbr
msigdb
yeast
14 months ago by
hamid.gaikani
▴ 80
0
votes
1
reply
685
views
Many MAF files in tcga case
maf
tcga
updated 14 months ago by
Zhenyu Zhang
★ 1.3k • written 14 months ago by
Beowulf
• 0
2
votes
2
replies
784
views
Optimising False Positive Detection in NGS Pipelines Using Mapping and Base Quality Scores
BaseQualityRankSumTest
14 months ago by
ManuelDB
▴ 110
0
votes
6
replies
918
views
Variant Sampling programm
variant-sampler
vsampler
14 months ago by
berndmann
• 0
2
votes
1
reply
498
views
RNA seq alignment issue
RNA-seq
updated 14 months ago by
Ram
45k • written 14 months ago by
Hashan
• 0
0
votes
1
reply
434
views
How to get all GO IDs of a specific GO term
GO
updated 14 months ago by
GenoMax
153k • written 14 months ago by
jet
• 0
0
votes
2
replies
854
views
How to use SNPlocs.Hsapiens.dbSNP150.GRCh38
TwoSampleMR
SNP
GWAS
14 months ago by
learner__lin2003
• 0
0
votes
0
replies
455
views
News:
Online course on Reproducibility Data Analysis with R
R
Github
Git
Reproducibility
Docker
14 months ago by
Physalia-courses
★ 2.6k
0
votes
2
replies
911
views
normalizing multiple conditions together or not
normalization
edgeR
14 months ago by
markus.glass
▴ 40
4
votes
4
replies
1.1k
views
MACS2 for multiple conditions in ATACseq analysis
mac2
14 months ago by
QX
▴ 80
3
votes
1
reply
1.3k
views
Right method to annotate genes on pangenome graph
pangenome
vg
updated 14 months ago by
colindaven
7.9k • written 14 months ago by
Quanyu
▴ 20
0
votes
0
replies
368
views
positional conservation scores
conservation-scores
FASTA
MSA
updated 14 months ago by
Ram
45k • written 14 months ago by
wannabio
• 0
4
votes
4
replies
1.2k
views
Increase the memory and core usage of R
R
updated 14 months ago by
Mensur Dlakic
★ 30k • written 14 months ago by
QX
▴ 80
2
votes
5
replies
1.3k
views
MetaTranscriptomics amount of viable reads
metagenomics
rna-seq
transcriptomics
updated 14 months ago by
andres.firrincieli
3.9k • written 14 months ago by
zjhennin
• 0
5
votes
0
replies
1.5k
views
Tutorial:
10 books got me started on bioinformatics
bioinformatics
computational-biology
updated 14 months ago by
Ram
45k • written 14 months ago by
Ming Tommy Tang
★ 4.7k
0
votes
1
reply
746
views
need help analyzing Geomx spatial transcriptomics data
spatialtranscriptomics
nanostring
geomx
updated 14 months ago by
4732b159
• 0 • written 19 months ago by
Cony Lab
• 0
12
votes
3
replies
1.3k
views
How to use GFF3 annotation to split genome fasta into gene sequence fasta in R
R
GFF3
fasta
genome
updated 14 months ago by
Ram
45k • written 14 months ago by
Chilly
★ 1.3k
0
votes
2
replies
901
views
Convert hifi_reads.bam to fastq for CellRanger
IsoSeq
CellRanger
MAS-Seq
14 months ago by
nwerry
• 0
0
votes
2
replies
949
views
Annotating enhancer elements (GRCh38)
annotation
features
enhancers
13 months ago by
eebloom
▴ 110
0
votes
0
replies
361
views
Molecular docking and molecular dynamics
Molecular-docking
molecular-dynamics
updated 14 months ago by
Ram
45k • written 14 months ago by
Under
• 0
0
votes
3
replies
842
views
Help with edgeR analysis
edgeR
RNA-seq
updated 13 months ago by
Raag
▴ 20 • written 14 months ago by
rb_99
• 0
0
votes
1
reply
623
views
Any body know how to convert CHR_BP to SNP rsid?
TwoSampleMR
SNP
GWAS
updated 14 months ago by
GenoMax
153k • written 14 months ago by
learner__lin2003
• 0
4
votes
9
replies
1.9k
views
Kallisto - Effect of Kmer size on quantification?
Kallisto
single-overhang
Kmer
RNA-seq
length
14 months ago by
jayeshkumarsundaram
▴ 10
0
votes
2
replies
692
views
Batch correction for protein data
proteomics
DESeq2
batch-correction
13 months ago by
4732b159
• 0
0
votes
1
reply
1.3k
views
Normalized enrichment Score (NES) cut-off
NES
GSEA
analysis
threshold
GO
updated 14 months ago by
GenoMax
153k • written 14 months ago by
shakyaram079
• 0
0
votes
1
reply
1.2k
views
Enrichment analysis guide for msu7 rice genome
transcriptome
KEGG
MSU7
rice
GOenrichment
updated 14 months ago by
白
• 0 • written 2.1 years ago by
sumitra.20
• 0
1
vote
4
replies
1.2k
views
Merging two sequencing datasets
NovaSeq
genomics
updated 13 months ago by
swbarnes2
15k • written 14 months ago by
laura.bertola
• 0
1
vote
6
replies
1.3k
views
header sequence interpretation
Illumina
fastq
short-read
updated 13 months ago by
Ram
45k • written 14 months ago by
Meghan.T
▴ 10
0
votes
0
replies
493
views
TCGAbiolinks: Accessing Matched Samples' Data Across -Omics Hierarchies
TCGAbiolinks
mixOmics
multi-omics
TCGA-BRCA
14 months ago by
Desmond
• 0
0
votes
2
replies
672
views
EditingSites for mm39
mouse
Genome-Browser
Mus-musculus
14 months ago by
alba
• 0
0
votes
1
reply
807
views
Don't understand three modes of TCGA STAR 2-pass
GDC
RNA-seq
TCGA
updated 14 months ago by
Zhenyu Zhang
★ 1.3k • written 14 months ago by
tomas4482
▴ 430
0
votes
2
replies
721
views
Getting A List Of Pfam Domains Involved in DNA-binding
Proteins
HMMER
Pfam
DNA-binding
14 months ago by
jet
• 0
0
votes
1
reply
651
views
Pangenome validation
pangenome
updated 12 months ago by
Uveyik
▴ 80 • written 14 months ago by
aaaniich
• 0
3
votes
2
replies
952
views
is that statistical correct to use DEseq2 for proteomics data
proteomics
DEseq2
updated 14 months ago by
ATpoint
89k • written 14 months ago by
QX
▴ 80
0
votes
0
replies
518
views
Cell Typist Providing different results between iterations
Python
Single-Cell
CellAnnotation
CellTypist
updated 14 months ago by
Ram
45k • written 14 months ago by
Manuel Sokolov Ravasqueira
▴ 110
2
votes
1
reply
981
views
How do I visualize variants from VCF file in IGV?
IGV
handbook
14 months ago by
Fanta
▴ 10
0
votes
2
replies
993
views
How can we identify if there are neighboring genes or overlapping promoter regions within the 1000 bp upstream of the transcription start site (TSS) …
TSS
TFBS
updated 14 months ago by
Ram
45k • written 14 months ago by
Cluster
• 0
0
votes
0
replies
430
views
Gene-pathway network with FDR or p value
clusterprofiler
14 months ago by
Chris
▴ 360
4
votes
7
replies
2.1k
views
Join command for the issue
join
linux
updated 14 months ago by
Ram
45k • written 3.7 years ago by
Confused_human
▴ 30
0
votes
1
reply
715
views
Absolute counts or relative abundance for BC distance matrix
metagenomics
microbiome
14 months ago by
mail2steff
▴ 70
0
votes
0
replies
431
views
The differences between pipelines for lncRNA identification
Cufflinks
StringTie
lncRNA
14 months ago by
ZZOYEA
▴ 20
0
votes
0
replies
474
views
News:
Online course: Genomic Data Visualization with R
Data-Visualisation
Genomic-Data
R
14 months ago by
Physalia-courses
★ 2.6k
3
votes
2
replies
4.3k
views
Tool:
VCF2PopTree: build a phylogenetic tree from a VCF file
VCF2Phylogenetictree
updated 14 months ago by
hewm2008
▴ 50 • written 4.5 years ago by
sankar2004
▴ 60
5
votes
3
replies
1.0k
views
temp directory as output in snakemake
directory
temp
snakemake
updated 14 months ago by
Jesse
▴ 880 • written 14 months ago by
hamarillo
▴ 80
0
votes
2
replies
977
views
Does Biopython.Blast allow you to read nucleotide sequences with ambiguous bases?
biopython
blast
updated 14 months ago by
Joe
22k • written 14 months ago by
Airhead
• 0
0
votes
0
replies
401
views
How many reads per cells are needed for splicing isoform analysis with Pac Bio long. read sequencing?
splicing
isoform
14 months ago by
jeremy.wen
• 0
0
votes
0
replies
407
views
Are there tools for protein family synteny searches?
pfam
interpro
synteny
14 months ago by
hopf
▴ 10
121,924 results • Page
85 of 2439
Recent Votes
Comment: Genome Assembly QC from BAM files
Answer: Understanding the relationship between hhr and a3m output of HHblits
Downsample BAM file to specific amount of reads
Answer: Downsample BAM file to specific amount of reads
Comment: SNP calling with bacterial assembled genome
Answer: Understanding the relationship between hhr and a3m output of HHblits
C: Annotation for gene-level analysis after stringtie
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Recent Replies
Comment: Understanding the relationship between hhr and a3m output of HHblits
by
Joe
22k
Nice detective work! :)
Comment: Hifiasm is getting killed while trying to assemble a genome
by
pranavdatar01
• 0
The SRA accession is SRX12366993
Comment: SNP calling with bacterial assembled genome
by
GenoMax
153k
> After I find some differences between the assembly and the reference, how can I decide confident variants without the depth? Don't think…
Comment: Orthofinder Not Mapping to Any Orthogroups
by
Philipp Bayer
8.9k
Did you check whether your species' fasta file is named correctly? From memory Orthofinder will pull in files ending in .fa and .fasta in t…
Comment: SNP calling with bacterial assembled genome
by
yesquokkan
• 0
Thank you for your kind answer. May I ask some following questions. However, I only have full access to assembled genomes, and some to ra…
Answer: Understanding the relationship between hhr and a3m output of HHblits
by
Andrew
▴ 10
Ok after reviewing the HHBlits source code I realize the issue is that the hhr file and the a3m file contain apples and oranges, and it doe…
Comment: Orthofinder Not Mapping to Any Orthogroups
by
saamhasan55
▴ 10
I checked the file and it's definitely proteins. I had previously run BUSCO on protein mode on the same file and got >90% completeness. I r…
Comment: Orthofinder Not Mapping to Any Orthogroups
by
saamhasan55
▴ 10
I ran BUSCO on the predicted proteome in protein mode and got >91% completeness. I also removed multiple isoforms from the same gene.
Comment: Help with Model
by
Stele
• 0
Hey, thanks for the reply! I think I didn't make the question very understandable. I do know how to code for this, the wall I have hit is *…
Comment: Orthofinder Not Mapping to Any Orthogroups
by
Mensur Dlakic
★ 30k
Not enough detail to make a definitive recommendation. Since this should not happen, an educated guess is that you are doing something wron…
Comment: Orthofinder Not Mapping to Any Orthogroups
by
Michael
56k
A reason may be that your gene prediction is off. Did you run BUSCO on your predicted proteome? If the gene prediction is ok, then you shou…
Comment: Genome Assembly QC from BAM files
by
GenoMax
153k
> Can you comment on these, If they look good ? More importantly how do these assemblies compare (contiguous/number of chromosomes/size) t…
Comment: TOPMed Imputation - More than 10000 allele switches
by
Qianshu
• 0
Hi, I have the same error with you, have you sorted it out yet? If you have, could you please share some? Thank you!
Comment: Genome Assembly QC from BAM files
by
colindaven
7.9k
yes they look excellent
Comment: Genome Assembly QC from BAM files
by
SomeOne
▴ 240
hello @colindaven I ran the INSPECTOR tool you mentioned on the genome assemblies. Below are stats for one of my sample (othere were simi…
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