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93 results • Page
2 of 2
Sort: Votes
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Votes
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0
votes
0
replies
67
views
supervised admixture
supervised
admixture
22 hours ago by
RT
▴ 10
0
votes
0
replies
61
views
Krona Pie-chart taxanomy IDs were not found warning. Taxonomy Classification Metagenomics
Classification
Metagenomics
Krona
Kraken2
19 hours ago by
Aytaç
• 0
0
votes
0
replies
49
views
Nomalization - TCGA, RNA-seq and Microarray
TCGA
RNA-seq
Nomalization
Microarray
14 hours ago by
jain72744
▴ 10
0
votes
0
replies
48
views
Allele specific expression of imprinted gens from 10x scRNA-seq data
scrna-seq
imprinted
10x
genes
14 hours ago by
singcell
• 0
0
votes
0
replies
53
views
Trouble converting tfam and tped to map and ped files
plink
ped
tfam
tped
map
12 hours ago by
Samantha
• 0
0
votes
2
replies
103
views
LncRNA Nomenclature
ENST
nomenclature
lncrna
GBB
ENSG
12 hours ago by
jain72744
▴ 10
0
votes
1
reply
107
views
When should I use R-MarkDown over R-Script ?
r
rscript
rmarkdown
updated 10 hours ago by
ATpoint
82k • written 14 hours ago by
Amr
▴ 160
0
votes
1
reply
83
views
Microbial Signal Transduction Database
MiST
updated 10 hours ago by
zx8754
11k • written 12 hours ago by
Shravani
• 0
0
votes
0
replies
48
views
input file in rmats
rmats
updated 10 hours ago by
zx8754
11k • written 12 hours ago by
Lambodarswain316
• 0
0
votes
0
replies
69
views
How do I calculate SE or P value if I only have BETA
prscsx
beta
se
pvalue
updated 10 hours ago by
zx8754
11k • written 21 hours ago by
curious_butterfly
• 0
0
votes
0
replies
51
views
How to convert Haps file to vcf file?
pre-phasing
GWAS
imputation
9 hours ago by
SeoGyun
• 0
0
votes
3
replies
201
views
Correlation Analysis
statistics
methylation
NGS
expression
updated 9 hours ago by
manaswwm
▴ 510 • written 3 days ago by
Researcher
▴ 30
0
votes
0
replies
50
views
How are score_weights calculated in this code?
cell
single
8 hours ago by
carolofharvest
▴ 40
0
votes
1
reply
56
views
Alignment of samples with spike-in
alignment
multimapping
RNA-seq
ChIP-seq
spike-in
updated 7 hours ago by
GenoMax
142k • written 7 hours ago by
maria.soler
• 0
0
votes
0
replies
35
views
Marker Features variance by cluster, sample, and treatment group
Seurat
scATAC-seq
features
Marker
ArchR
4 hours ago by
naomiboldon
• 0
0
votes
3
replies
91
views
How to format "I" and "D" in vcf version 4.2 for liftover analysis in GATK
gatk
vcf
converter
liftover
updated 4 hours ago by
Giulio Genovese
▴ 390 • written 5 hours ago by
Omics data mining
▴ 260
0
votes
5
replies
144
views
Too many unpaired forward reads found by Trimmomatic
Trimmomatic
2 hours ago by
SilhouetteQ
• 0
0
votes
0
replies
17
views
Practical Haplotype Graph v2 not finding correct paths
Pangenome
PHG
graph
1 hour ago by
beantkapoor16
• 0
0
votes
6
replies
432
views
Differential Expression Analysis using DESeq2 in R
deseq2
R
updated 6 days ago by
swbarnes2
14k • written 7 days ago by
Erina
• 0
0
votes
2
replies
211
views
fastq screen aligner no specified.
BWA
Bowtie2
FastqScreen
updated just now by
GenoMax
142k • written 6 days ago by
Ximena
• 0
0
votes
0
replies
136
views
Empty table plot using plotGseaTable()
FGSEA
6 days ago by
Chris
▴ 280
0
votes
2
replies
254
views
Downloading older version of a tool
Alignment
tools
6 days ago by
Ruqaiya
• 0
0
votes
1
reply
202
views
filtering before dada2
bbduk
qiime2
dada2
metagenomic
updated 6 days ago by
Ram
43k • written 6 days ago by
Valentina
• 0
0
votes
1
reply
237
views
Extracting mutation status from MAF files - TCGA
TCGA
maf
mutation
updated 6 days ago by
Thanujay S
• 0 • written 7 days ago by
yahn
• 0
0
votes
0
replies
156
views
Homer motif analysis
Homer
6 days ago by
daffodil
▴ 10
0
votes
0
replies
121
views
Clarification on StringTie's `--merge` parameters
stringtie
stringtie-merge
5 days ago by
DGTool
• 0
0
votes
0
replies
117
views
Looking for phytopathogenic, Nitrogen-Fixing, and Growth-Promoting databases for Metagenomic Analysis
Bacteria
Metagenomics
Database
5 days ago by
Christopher
• 0
0
votes
0
replies
128
views
Mitogenomes gap closure and making circular genome
gapclosure
Mitogenomes
validation
circulargenome
5 days ago by
KHURRAM SHAHZAD
• 0
0
votes
1
reply
225
views
Help with DGEList function
DGEList
R
updated 4 days ago by
marco.barr
▴ 100 • written 6 days ago by
Natali
• 0
0
votes
0
replies
118
views
How to implement an IGV to streamlit app?
python
streamlit
igv
4 days ago by
avigail.shnaider
• 0
0
votes
1
reply
261
views
creating batch colum for batch correction
batch-correction
combat
4 days ago by
Expert
▴ 10
0
votes
0
replies
115
views
Error while loading model of Spatial data deconvolution using cell2location
Python
cell2location
updated 4 days ago by
Ram
43k • written 4 days ago by
sidrah.maryam
▴ 50
0
votes
0
replies
101
views
Normalizing AMR gene count data
abundance
RGI
updated 4 days ago by
Ram
43k • written 4 days ago by
arshad1292
▴ 100
0
votes
0
replies
104
views
vdjtools
vdjtools
4 days ago by
yueli7
▴ 250
0
votes
0
replies
110
views
Cox Model with interaction item interpretation
Cox
4 days ago by
Bine
▴ 60
0
votes
0
replies
104
views
Cellphonedb results
cpdb
visulization
cellphonedb
3 days ago by
piotto
▴ 20
0
votes
0
replies
108
views
Get Paired TCRa/b from MIXCR
python
r
mixcr
tcr_seq
3 days ago by
Scott McKay
▴ 30
0
votes
0
replies
180
views
CellPhoneDB results
cellphonedb
cpdb
cell_surface_proteins
updated 3 days ago by
GenoMax
142k • written 10 weeks ago by
piotto
▴ 20
0
votes
4
replies
386
views
Highest variable features in single cell data
single-cell
3 days ago by
carolofharvest
▴ 40
0
votes
0
replies
107
views
Imputation of missing genotypes
panel
beagle
imputation
3 days ago by
analyst
▴ 50
0
votes
1
reply
283
views
16S rRNA microbiome differential abundance analysis with DESeq2 finds same microbial Genus in both groups.
microbiome
16S
DESeq2
updated 3 days ago by
andres.firrincieli
3.6k • written 4 days ago by
Antonio
• 0
0
votes
2
replies
236
views
RNA editing sites based on DNA seq and RNA seq
RNA-editing
3 days ago by
Ahiad Chen Zion
• 0
0
votes
3
replies
166
views
trying to count a pattern in my fastq file using bbduk
java
bbduk
bbmap
fastq
updated 3 days ago by
GenoMax
142k • written 3 days ago by
Assa Yeroslaviz
★ 1.8k
93 results • Page
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Recent Replies
Comment: fastq screen aligner no specified.
by
Ximena
• 0
Thank u so much, my OS is linux. I will try your advice.
Comment: In IGV is this a heterogeneous mutation or false call?
by
Tuck898
• 0
No worries, I can completely appreciate that. I am having investigations similar to a condition causes by the RYR2 gene and was wondering i…
Comment: In IGV is this a heterogeneous mutation or false call?
by
Pierre Lindenbaum
161k
> RYR1 underneath although I was originally looking at the RYR2 gene. Sorry to sound stupid but does this make sense to what I've previousl…
Comment: In IGV is this a heterogeneous mutation or false call?
by
Tuck898
• 0
When click the blat it brings me to chr19 and mentions the RYR1 underneath although I was originally looking at the RYR2 gene. Sorry to sou…
Comment: In IGV is this a heterogeneous mutation or false call?
by
Tuck898
• 0
Thanks for that! I'll try and have a look and see what is amiss if I can... In your opinion what do you feel is wrong in my alignment from…
Comment: In IGV is this a heterogeneous mutation or false call?
by
Pierre Lindenbaum
161k
yeah.. look at that, there is something wrong in your alignment, many reads were mapped in a location but they are all clipped, so somethin…
Comment: Custom Reference panel creation for data imputation from .vcf files
by
analyst
▴ 50
Hi [Kevin][1]! I have 80 samples of GBS data. I have called variants through GATK pipeline. Now I have to perform imputation. Do I need …
Comment: In IGV is this a heterogeneous mutation or false call?
by
Tuck898
• 0
Ah I've just found 'show soft clipped bases' and this is what comes up... how come it is all greyed out? ![enter image description here][…
Comment: In IGV is this a heterogeneous mutation or false call?
by
Tuck898
• 0
I've just displayed clipped bases and this is what it shows. Does this look right? ![enter image description here][1] ![enter imag…
Comment: In IGV is this a heterogeneous mutation or false call?
by
Tuck898
• 0
Hi, I really appreciate you taking the time to reply. I'm still learning with IGV and sorry to sound very inexperienced but how would I che…
Answer: In IGV is this a heterogeneous mutation or false call?
by
Pierre Lindenbaum
161k
there is a clear shift in the depth just close to this mutation, you should set IGV to display the clipped bases + check if there is a DUP …
Comment: Too many unpaired forward reads found by Trimmomatic
by
SilhouetteQ
• 0
Using fastp, I found that the adapter sequence for the forward read is corresponding to Trans2_rc in the NexteraPE-PE.fa, while for the re…
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…
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