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804 results • Page
4 of 17
Sort: Votes
Rank
Views
Votes
Replies
3
votes
4
replies
415
views
Why gatk VariantAnnotator required bam and coverage files
gatk
VariantAnnotator
21 days ago by
QX
• 0
3
votes
3
replies
751
views
KissDE and batch effect
kissDE
kissplice
24 days ago by
david.b.rombaut
▴ 10
3
votes
2
replies
419
views
Extract protein sequence
fasta
alignment
blast
16 days ago by
anna
▴ 20
3
votes
3
replies
367
views
Sequence read length shorter than flow cell specification
illumina
NGS
sequencing
updated 21 days ago by
swbarnes2
14k • written 21 days ago by
M
• 0
3
votes
8
replies
6.6k
views
7 follow
GATK genomicsDBimport intervals for WGS
gatk
genomicsdbimport
updated 14 days ago by
Sd
• 0 • written 5.1 years ago by
Nicolas Rosewick
11k
3
votes
3
replies
368
views
genome assembly records not present in assembly_summary.txt
ncbi
bacteria
assembly
updated 20 days ago by
GenoMax
142k • written 20 days ago by
sapuizait
▴ 10
3
votes
1
reply
213
views
Long reads and fixing of mate-pair issues/marking duplicates with samtools
mate-pair
samtools
alignment
updated 3 days ago by
aw7
▴ 300 • written 8 days ago by
Zeng Hao
▴ 40
3
votes
2
replies
167
views
Details on salmon index
Salmon
updated 13 hours ago by
Rob
6.6k • written 20 hours ago by
Lorenzo
• 0
3
votes
2
replies
1.2k
views
DESeq2 design and Batch effects
RNA-Seq
batch-effect
DESeq2
updated 29 days ago by
Ram
43k • written 4.5 years ago by
baldissera152
▴ 10
2
votes
2
replies
1.6k
views
Combining control samples from 2 separate studies. Model matrix for batch effect?
gene-expression
R
limma
batch-effect
model-matrix
updated 28 days ago by
Ram
43k • written 7.3 years ago by
tolgaturant
▴ 20
2
votes
5
replies
423
views
How to trim transcripts using information from NCBI contamination screen report
RNAseq
assembly
transcriptome
contamination
20 days ago by
Lada
▴ 30
2
votes
4
replies
719
views
Count all variants from vcf file
variants
vcf
Count
updated 9 days ago by
Pierre Lindenbaum
161k • written 21 months ago by
t.ali
• 0
2
votes
3
replies
500
views
Sheep reference genome remapping coordinates
reference
remap
sheep
coordinates
genome
28 days ago by
valentinatsar
• 0
2
votes
3
replies
322
views
Help with choosing a model species for Augustus for a de novo assembled genome.
augustus
annotation
assembly
genome
updated 13 days ago by
dthorbur
★ 2.0k • written 13 days ago by
Vijith
▴ 30
2
votes
5
replies
566
views
Tissue-specific DEG analysis with DEseq2
DEseq2
RNA-seq
DEG
R
updated 4 days ago by
arctic
▴ 40 • written 13 days ago by
M.
▴ 30
2
votes
3
replies
844
views
Issues with Mixture file when using CIBERSORTx
Deconvolution
CIBERSORTx
updated 12 days ago by
vjanve
• 0 • written 7 months ago by
mateomejias
• 0
2
votes
5
replies
404
views
Importing a fastq file
Fastq
updated 7 days ago by
size_t
▴ 120 • written 7 days ago by
oumo
• 0
2
votes
3
replies
272
views
Finding variants within a subset of a BAM file
variant
calling
2 days ago by
ramiro.barrantes
• 0
2
votes
4
replies
389
views
Should I use unpaired reads from trimmomatic
RNA-seq
QC
Trimmomatic
updated 23 days ago by
swbarnes2
14k • written 24 days ago by
dxj294
• 0
2
votes
4
replies
4.5k
views
Differential Expression Analysis with monocle and batch effect correction
single-cell
RNA-Seq
batch-effect
updated 29 days ago by
Ram
43k • written 6.0 years ago by
Poorya Parvizi
▴ 60
2
votes
7
replies
1.4k
views
6 follow
Differential Expression using Isoseq-supplemented reference transcriptome
RNA-Seq
Salmon
Isoseq
updated 18 days ago by
Gordon Smyth
★ 7.2k • written 8 months ago by
Calum
▴ 10
2
votes
2
replies
1.1k
views
Can we directly use batch corrected gene expression (Bulk RNA-seq) for further downstream analyses?
RNA-Seq
batch-effect
updated 28 days ago by
Ram
43k • written 5.1 years ago by
tigeradab
▴ 60
2
votes
1
reply
232
views
Failed to open VCF file
GATK
sentieon
BWA-MEM
updated 5 days ago by
Pierre Lindenbaum
161k • written 5 days ago by
melissachua90
▴ 70
2
votes
2
replies
310
views
p-value in CIBERSORT
CIBERSORT
p-value
15 days ago by
michelafrancesconi9
▴ 20
2
votes
2
replies
217
views
MA plot of shrunken fold change
MA-plot
Deseq2
updated 16 days ago by
ATpoint
82k • written 16 days ago by
Sudip
• 0
2
votes
5
replies
266
views
What does the 'E%' represent in BUSCO results?
BUSCO
updated 3 days ago by
Philipp Bayer
8.5k • written 3 days ago by
林明德
• 0
2
votes
5
replies
536
views
Fetch table from clinvar database according to a list of rsid
python
clinvar
perl
18 days ago by
ashaneev07
▴ 20
2
votes
1
reply
2.1k
views
How to make batch univariate cox analysis for list
univariate-cox-analysis
updated 28 days ago by
Ram
43k • written 4.8 years ago by
BioLite
▴ 20
2
votes
2
replies
428
views
differential gene expression analysis when not all samples have an untreated counterpart
differential-expression
edgeR
28 days ago by
nhaus
▴ 360
2
votes
2
replies
242
views
Raw counts using stringtie
stringtie
RNA-seq
updated 13 days ago by
GenoMax
142k • written 13 days ago by
ahmad.sajad4541
• 0
2
votes
3
replies
208
views
RSeQC : infer_experiment.py Error: Could not retrieve index file
RSeQC
RNA-Seq
updated 2 days ago by
Ram
43k • written 2 days ago by
Prawesh
• 0
2
votes
6
replies
3.8k
views
Treatment VS Control in Single Cell RNAseq analysis
Single Cell
RNAseq
DE Analysis
Treatment
Control
updated 21 days ago by
ATpoint
82k • written 3.9 years ago by
grayapply2009
▴ 280
2
votes
5
replies
535
views
Marking duplicates using UMIs
Deduplication
UMI
updated 24 days ago by
i.sudbery
19k • written 26 days ago by
Lipika
• 0
2
votes
14
replies
2.9k
views
6 follow
CNVKIT - unable to produce scatter and diagram pdfs
cnvkit
updated 2 days ago by
Anitha
• 0 • written 4.8 years ago by
ww22runner
▴ 60
2
votes
0
replies
165
views
Herald:
The Biostar Herald for Monday, May 06, 2024
herald
10 days ago by
Biostar
2.8k
2
votes
5
replies
2.5k
views
identifying transgene insertion site in WGS
WGS
insertion site
trangene
de-novo
soap
updated 8 days ago by
Cameron.walker9900
• 0 • written 5.1 years ago by
Assa Yeroslaviz
★ 1.8k
2
votes
2
replies
393
views
Hide positions in alignment with 99% "–" characters to ignore single sequence insertions?
alignment
gaps
updated 19 days ago by
Jesse
▴ 770 • written 21 days ago by
Broccoli
• 0
2
votes
3
replies
995
views
Method to detect genome doubling
CNV
genome doubling
updated 24 days ago by
LauferVA
4.2k • written 4.5 years ago by
CY
▴ 750
2
votes
2
replies
195
views
Genome Visualization Tools
bacterial
genome
updated 2 days ago by
GenoMax
142k • written 2 days ago by
dlera.lozano
▴ 10
2
votes
9
replies
692
views
Filtering Multi-sample VCF file for all except one Genotype
variant
SNP
VCF
updated 1 day ago by
Pierre Lindenbaum
161k • written 9 days ago by
schmince
• 0
2
votes
3
replies
183
views
ggrepel function: geom_text_repel()
ggplot2
ggrepel
R
updated 6 hours ago by
Ram
43k • written 1 day ago by
sooni
▴ 20
2
votes
0
replies
155
views
News:
course on Landscape Genomics at the EPFL in Lausanne (June 17-21)
LandscapeGenomics
SNPs
LocalAdaptation
GIS
7 days ago by
carlopecoraro2
★ 2.5k
2
votes
7
replies
5.3k
views
6 follow
Memory usage of picard Samsort
Picard
SortSam
updated 27 days ago by
ATpoint
82k • written 7.2 years ago by
boymin2020
▴ 80
2
votes
6
replies
377
views
BWA alignment
Samtools
bam
updated 2 days ago by
a.alnawfal.1992
▴ 260 • written 4 days ago by
Vahid
• 0
2
votes
4
replies
2.7k
views
When to use .vcf or .gvcf files from GATK HaplotypeCaller?
indel
gatk
calling
snp
variant
updated 17 days ago by
Medhat
9.7k • written 2.0 years ago by
Vitor1
▴ 120
2
votes
3
replies
401
views
Editing Human Reference Genome by adding a CDS
gff
agat
transcriptome
updated 29 days ago by
Michael
54k • written 29 days ago by
LDT
▴ 340
2
votes
2
replies
334
views
How to calculate identity percentage between proteins contained in a FASTA file?
protein
FASTA
alignment
updated 22 days ago by
Ram
43k • written 23 days ago by
v.berriosfarias
▴ 140
2
votes
2
replies
155
views
Single-cell ambient RNA correction: SoupX vs decontX contamination fraction
single-cell
ambient-RNA
updated 9 hours ago by
Ram
43k • written 12 hours ago by
txema.heredia
▴ 130
2
votes
3
replies
276
views
error in fun(x((i)), ...) : only defined on a data frame with all numeric alike variables
studio
Cibersort
R
3 days ago by
Azra
▴ 10
2
votes
2
replies
480
views
Using vg gamsort with naive sorting algorithm
gamsort
vg
updated 23 days ago by
Pierre Lindenbaum
161k • written 8 months ago by
AshleeThomson
▴ 80
804 results • Page
4 of 17
Recent Votes
Answer: ggrepel function: geom_text_repel()
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ATAC-seq sample normalization
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Comment: How to extract cells of different species after mapping with combined genome?
by
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I think this method should be applicable to all high-throughput single-cell RNA-seq platforms. Although the method of determining cell spec…
Comment: BiomartException: Query ERROR for existing dataset in BioMart
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The dataset you want (taestivum_eg_gene) exists within the "plants_mart" schema, not the default schema. Your current code assumes the defa…
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You could use [this][1] [1]: https://ggplot2.tidyverse.org/reference/geom_segment.html
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Thank you for your reply. I am not very much sure about this RG. Can you explain me a bit?
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It seems that Alexandrov's [structural variant and copy number signatures][1] estimated by the [SigProfiler software ecosystem][2] aren't c…
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Then you may want to see if a program like `lastz` ([**LINK**][1]) may be useful. [1]: https://github.com/lastz/lastz
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What is the purpose of this tool? I have `~/bin` in my $PATH and I soft-link all executables I need to that location so why install a new t…
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Can you try this? library(dplyr) seuratobj@meta.data <- seuratobj@meta.data %>% mutate(seurat_clusters = recode(seurat_clu…
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by
kilcdincer
▴ 10
Thank you for the response but it does not change anything.
Comment: Merge clusters in Seurat UMAP
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bk11
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I have not tested but you could try something like below- seuratobj$seurat_clusters[seuratobj$seurat_clusters==5]=0 seuratobj$seur…
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I know about it, isn't there a simple C++ static binary?
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needle is great! but it does not handle sequences of 100k or so.
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43k
Please use the formatting bar (especially the `code` option) to present your post better. You can use backticks for inline code (\`text\` b…
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▴ 130
The point is that you need to feed the ambient algorithm a clustering list as input. This way, it checks for genes present in the soup vs g…
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