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121,395 results • Page
583 of 2428
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Votes
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0
votes
1
reply
890
views
Extracting variations in the gene regions and from 100 bp of gene boundary from multiple VCF files
VCF
Variations
updated 3.8 years ago by
Tm
★ 1.1k • written 3.8 years ago by
VenGeno
▴ 100
0
votes
0
replies
521
views
Codeml giving different chi2 values when reducing the number of sequences
PAML
CODEML
3.8 years ago by
Amay
▴ 10
0
votes
0
replies
609
views
VcfSampleCompare - empty output with warnings
VcfSampleCompare
empty
warnings
3.8 years ago by
Michal Nevo
▴ 140
0
votes
0
replies
688
views
PCA on pooled and single individuals
PCA
analysis
component
pooled
principal
structure
samples
population
3.8 years ago by
javiergandasegui
• 0
0
votes
0
replies
603
views
KAAS: Limiting The Genes Associated With a Pathway to a Certain Species
KEGG
KAAS
pathway
metabolic
3.8 years ago by
adhamzul
▴ 20
4
votes
5
replies
3.4k
views
6 follow
TopHat error: IOError [errno 2] No such file or directory: '-o'
RNA-Seq
rna-seq
alignment
software error
updated 6.2 years ago by
Kristoffer Vitting-Seerup
★ 4.2k • written 6.2 years ago by
lishen0709
• 0
0
votes
0
replies
624
views
Extract peptide information from proteomics data
proteomics
peptide
3.8 years ago by
Gene_MMP8
▴ 240
0
votes
0
replies
416
views
linking RNA-seq data with GWAS study
ngs
3.8 years ago by
hafiz.talhamalik
▴ 350
11
votes
7
replies
15k
views
How to include/keep only the samples in a list in VCF.gz file?
vcf
samples
bcftools
updated 2.5 years ago by
Pierre Lindenbaum
166k • written 6.9 years ago by
DanielC
▴ 210
0
votes
0
replies
898
views
What is a good Standardized Beta/standardized regression coefficient in a genetics study?
regression
genetics
genomics
updated 2.2 years ago by
Ram
45k • written 3.8 years ago by
jon.klonowski
▴ 210
0
votes
0
replies
872
views
Job:
Postdoc at Stanford working on mobile health device data from My Heart Counts
ai
science
device
mhealth
data
3.8 years ago by
hershman
▴ 40
2
votes
2
replies
972
views
Download nucleotide sequence with locus_tag
SEQUENCE
LOCUS_TAG
NUCLEOTIDE
NCBI
3.8 years ago by
DJ_MB
• 0
6
votes
13
replies
8.0k
views
9 follow
VCF file phasing by SHAPEIT
vcf
phasing
whole genome
shapiet
updated 3.8 years ago by
4galaxy77
2.9k • written 6.5 years ago by
seta
★ 1.9k
0
votes
1
reply
1.1k
views
Differential Gene Expression after batch correction with DESC?
DESC
scRNAseq
batch-effect
updated 9 months ago by
Ram
45k • written 3.8 years ago by
skjw1029
▴ 80
2
votes
3
replies
1.8k
views
how htseq-count counts unstranded RNA-seq data
htseq-count
RNA-seq
stranded
updated 3.8 years ago by
swbarnes2
15k • written 3.8 years ago by
wiscoyogi
▴ 40
0
votes
0
replies
557
views
Impute expression from bulk ATAC data
RNA
Imputation
ATAC
3.8 years ago by
kvshamsudheen
▴ 120
1
vote
1
reply
922
views
how to apply DE-kupl in my data for differential expression ?
DE-kupl
DE
updated 3.8 years ago by
ATpoint
88k • written 3.8 years ago by
m90
▴ 30
5
votes
7
replies
4.3k
views
Signac CallPeaks from multiple fragment files
Seurat
Macs2
Signac
3.7 years ago by
LacquerHed
▴ 30
0
votes
0
replies
604
views
PDBePISA calls monomers heteromers, how can one programmatically correct this downstream
PDBe
quaternary
PISA
structure
3.8 years ago by
plberry
▴ 30
1
vote
4
replies
1.7k
views
Demultiplexing with Linux
Demultiplexing
Linux
updated 3.8 years ago by
cpad0112
21k • written 3.8 years ago by
Nic
• 0
1
vote
1
reply
1.9k
views
makeblastdb Bus error
bus-error
blast
updated 12 months ago by
Ram
45k • written 3.8 years ago by
860101959
▴ 10
3
votes
10
replies
4.8k
views
6 follow
How do I match my transcript ID's from NCBI to the corresponding gene ID's to enable tximport into R?
Salmon
tximport
RNA-Seq
R
updated 2.9 years ago by
GenoMax
152k • written 3.8 years ago by
robeaumont
• 0
0
votes
2
replies
2.7k
views
How to change the track background color of IGV
IGV
3.8 years ago by
changxu.fan
▴ 80
0
votes
7
replies
1.7k
views
sortsam. picard
picard
updated 3.8 years ago by
Ram
45k • written 3.8 years ago by
munche17live
• 0
0
votes
0
replies
622
views
Pathway enrichment for draft gene names
pathway-enrichment
updated 24 months ago by
Ram
45k • written 3.8 years ago by
margot.27.muller
▴ 30
1
vote
2
replies
1.6k
views
HTSeq-count TruSeq RNA Exome Lib Prep
HTseq
strandness
TruSeqRNAExome
nofeatures
3.8 years ago by
tdfyoder
▴ 40
0
votes
0
replies
1.6k
views
Job:
Science Infrastructure Manager
management
infrastructure
project
Science
3.8 years ago by
EMBL Recruitment
▴ 30
1
vote
2
replies
1.1k
views
Accuracy Assembly's contigs
NGS
Assembly
whole
genome
Velvet
3.8 years ago by
askari.arezou94
▴ 30
0
votes
0
replies
643
views
Non-symmetric MA-plot (DESeq2)
MA-plot
DESeq2
3.8 years ago by
mdidish
• 0
4
votes
7
replies
2.7k
views
Inferring CNVs from BAM files with SAMTools depth
samtools
bam
wes
wgs
cnv
updated 3.8 years ago by
German.M.Demidov
★ 3.0k • written 3.8 years ago by
Sammy
▴ 30
1
vote
1
reply
912
views
Base recalibration -Java run time error and no sequence dictionary
base
GATK
NGS
recalibration
updated 3.8 years ago by
brunobsouzaa
▴ 840 • written 3.8 years ago by
priya.bmg
▴ 70
0
votes
1
reply
828
views
EQTL analysis
sQTL
eQTL
and
updated 3.8 years ago by
Carambakaracho
★ 3.3k • written 3.8 years ago by
Nai
▴ 50
0
votes
1
reply
807
views
Manhattan Plot in R with 100 non-numeric contigs and chromosomes
contigs
chromosomes
R
Manhattan
non-numeric
updated 3.8 years ago by
zx8754
12k • written 3.8 years ago by
Michal Nevo
▴ 140
1
vote
2
replies
3.1k
views
Filter on Allele Balance using BCFTools
bcftools
allele
filter
balance
updated 3.6 years ago by
Shicheng Guo
★ 9.6k • written 3.8 years ago by
sumudu_rangika
▴ 50
6
votes
9
replies
2.9k
views
Identification of transcription factors from a list of DEGs
DEGs
TFs
3.8 years ago by
navamikrishna99
▴ 10
1
vote
0
replies
1.1k
views
Job:
Bioinformatician — Biological data and network analysis
network-analysis
Biological-data
updated 2.5 years ago by
Ram
45k • written 3.8 years ago by
EMBL Recruitment
▴ 30
0
votes
1
reply
858
views
how to find interference residue
protein
updated 3.8 years ago by
Mensur Dlakic
★ 29k • written 3.8 years ago by
Mo
▴ 920
0
votes
0
replies
604
views
Error in reading the annotation files
PyRadiomics
Python
3.8 years ago by
mxz707
• 0
3
votes
14
replies
4.1k
views
STAR split reads into two strands
rnachip
stranded
split
STAR
3.8 years ago by
Alexander
• 0
2
votes
7
replies
2.4k
views
fastq file format
fastq
NGS
3.8 years ago by
Vladimir Leshuk
▴ 50
2
votes
2
replies
1.4k
views
Finding sequence family specific primers using DECIPHER
DECIPHER
PCR
primer
3.8 years ago by
Marcel
• 0
0
votes
0
replies
844
views
Best approach to finding correlation between two genes from MAGIC imputed single-cell RNA-seq data
genes
MAGIC
single-cell
corrolation
Seurat
3.8 years ago by
Stevens
▴ 30
0
votes
5
replies
2.3k
views
How to convert mapping bam file to fastq without loseing the mapping information
bedtools
bamtofastq
samtools
updated 3.8 years ago by
GenoMax
152k • written 3.8 years ago by
btx288
• 0
0
votes
0
replies
823
views
ICA - Reconstruction Errors
ICA
Omics
ML
updated 2.3 years ago by
Ram
45k • written 3.8 years ago by
Esra
• 0
0
votes
3
replies
1.3k
views
Assessing how similar/ different of activated pathways between multiple groups of samples
pathway
correlation
test
hypothesis
updated 3.8 years ago by
LauferVA
4.7k • written 3.8 years ago by
cwwong13
▴ 40
1
vote
2
replies
1.8k
views
Variant Calling Heterozygous Reference Alleles
alignment
vcf
gatk
variant
SNP
calling
updated 3.8 years ago by
LauferVA
4.7k • written 3.8 years ago by
mti193
▴ 10
0
votes
0
replies
869
views
BEDPE file for ENCODE 3D chromatin structure data
BEDPE
3.8 years ago by
arsala521
▴ 60
3
votes
1
reply
6.3k
views
how do I add a title to an Upset plots
Upset
plots
R
updated 3.8 years ago by
seidel
11k • written 3.8 years ago by
peter.berry5
▴ 60
0
votes
1
reply
1.3k
views
News:
Databricks Runtime for Genomics (Deprecated)
Runtime
Databricks
Genomics
updated 3.8 years ago by
GenoMax
152k • written 3.8 years ago by
Shicheng Guo
★ 9.6k
5
votes
12
replies
5.7k
views
weird MAplot or volcano plot of DESeq2 diff result
RNA-seq
DESeq2
3.8 years ago by
shangguandong1996
▴ 30
121,395 results • Page
583 of 2428
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Answer: Should I perform integration to correct batch effects?
Should I perform integration to correct batch effects?
Answer: Batch correction in TNBC epithelial cells
Answer: When should I NOT apply batch correction for my single-cell RNAseq data?
Answer: Should I perform integration to correct batch effects?
Answer: Batch correction in TNBC epithelial cells
Comment: convert raw counts to TPM
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Comment: Single-cell RNA Sequencing - transcript abundance estimation using Alevin-Fry
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7.1k
The main issue is that there will be an inherent lack of information (due to the aforementioned 3' bias) in tagged-end data. Nonetheless, …
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As per the manual, `FRAG` is specific for scATAC-seq while the other option is generic.
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