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11,722 results • Page
3 of 235
Sort: Rank
Rank
Views
Votes
Replies
3
votes
3
replies
238
views
Unexpected read length from NGS
NGS
Illumina
4 days ago by
QX
• 0
1
vote
7
replies
406
views
samtools write-index
samtools
2 days ago by
R.L.
• 0
2
votes
3
replies
318
views
How do we do quantification using stringtie merge option for all the merged samples generated.
stringtie
quantification
1 day ago by
Varsha
• 0
3
votes
2
replies
185
views
How to interpret this plotMDS of three disease clusters?
microarray
plotMDS
DEGs
updated 5 days ago by
ATpoint
82k • written 5 days ago by
egascon
• 0
0
votes
0
replies
94
views
GWAS or QTL mapping in RIL population
GWAS
RIL
5 days ago by
韩雨
• 0
0
votes
0
replies
97
views
VEP annotation tool: "." isn't numeric in addition (+)
VEP
VCF
updated 5 days ago by
Ram
44k • written 5 days ago by
emmanouil.a
▴ 120
11
votes
13
replies
6.8k
views
7 follow
log2 fold change in RNA-seq analysis
fold
log2
change
updated 5 days ago by
May Ling
• 0 • written 2.4 years ago by
wmsalsah
▴ 10
0
votes
1
reply
273
views
GWAS Phenotypes
GWAS
updated 5 days ago by
韩雨
• 0 • written 6 weeks ago by
solomoncharles77
▴ 90
5
votes
4
replies
5.2k
views
6 follow
Classic threshold for log2 fold change in RNA-seq experiment
RNA-Seq
updated 5 days ago by
May Ling
• 0 • written 3.9 years ago by
Mozart
▴ 330
1
vote
1
reply
140
views
Cellranger-multi : Demultiplexing and Analyzing 5’ Immune Profiling Libraries Pooled with Hashtags
5InmuneProfiling
nf-core
scRNAseq
cellranger-multi
Nextflow
updated 5 days ago by
GenoMax
142k • written 5 days ago by
azeu
▴ 10
0
votes
0
replies
66
views
Assigning Micro-C read pairs to nucleosomes called from MNase-seq data?
Hi-C
MNase-Seq
5 days ago by
Linus
• 0
7
votes
3
replies
13k
views
Z score in RNAseq
RNA-Seq
Zscore
updated 5 days ago by
Akash D
▴ 60 • written 6.5 years ago by
rob.costa1234
▴ 310
0
votes
1
reply
157
views
Free AI for R programming
R
updated 5 days ago by
Ram
44k • written 5 days ago by
mohamadzare6022
▴ 10
7
votes
13
replies
852
views
7 follow
Forum:
Ideal PC configurations and operating system for bioinformatics laboratory
PC
updated 5 days ago by
i.sudbery
19k • written 5 weeks ago by
Estevão
▴ 10
0
votes
0
replies
106
views
Extracting haplotype-specific annotations from splicing graph
vg
6 days ago by
Juhyun
• 0
0
votes
0
replies
97
views
miloR - object 'as.SimpleList' of mode 'function' was not found when running calcNhoodDistance
scRNA-seq
seurat
miloR
6 days ago by
shuaizh117
▴ 10
0
votes
0
replies
98
views
Phyloseq returning black bars for plot_bar
phyloseq
bioconductor
R
6 days ago by
Jacob
• 0
3
votes
8
replies
887
views
Random Access remote BAM files
htslib
BAM
updated 6 days ago by
a.penatauber
• 0 • written 3 months ago by
Lucas R.F.
▴ 20
0
votes
0
replies
99
views
Cancer vs Normal Cell Classification Based on SNVs
cancer
6 days ago by
dglad
• 0
0
votes
4
replies
231
views
merge overlaps and remove non overlap genomic windows
BED
intersection
overlap
6 days ago by
reza
▴ 300
0
votes
1
reply
150
views
Small secondary peak for per sequence GC content - FASTQC results (bulk RNA-seq)
RNAseq
updated 6 days ago by
GenoMax
142k • written 6 days ago by
Fossil
• 0
1
vote
2
replies
251
views
Construction of circos plot from WGS data
WGS
Circos
5 days ago by
Anitha
▴ 10
1
vote
3
replies
244
views
Trimmomatic running but files containing purged reads are empty
fastqc
fastq
trimmomatic
updated 6 days ago by
GenoMax
142k • written 6 days ago by
Wilber0x
▴ 50
0
votes
0
replies
111
views
How to find nucleotide changes and the predicted effect when comparing two genomes
BLAST
alignment
updated 6 days ago by
Ram
44k • written 6 days ago by
Melissa
• 0
5
votes
3
replies
216
views
FastQC interpretation - 16S sequencing
interpretation
amplicon
Fastqc
16S
updated 6 days ago by
GenoMax
142k • written 6 days ago by
Christopher
▴ 10
0
votes
0
replies
126
views
Subset of ATAC-seq peaks has high variance
atac-seq
edgeR
R
normalization
5 days ago by
Tim
• 0
2
votes
6
replies
336
views
How to get the ratio of allele counts from GATK derived VCF file?
Freebayes
GATK
SNP
VCF
5 days ago by
anikcropscience
▴ 230
0
votes
0
replies
104
views
KEGG pathway enrichment analysis in Zea mays with R
KEGG
Zea-mays
R
updated 6 days ago by
Ram
44k • written 6 days ago by
letizia.ottaviani
• 0
0
votes
6
replies
298
views
from CRAM to fastq
FASTQ
WGS
CRAM
updated 6 days ago by
ATpoint
82k • written 6 days ago by
machaalani29
• 0
0
votes
0
replies
104
views
News:
Bioinformatic Analysis of Transposable Elements course
Genome-Annotation
TE
Manual-Curation
Transposable-Elements
updated 6 days ago by
Ram
44k • written 6 days ago by
carlopecoraro2
★ 2.5k
0
votes
1
reply
134
views
No output when converting transcript IDs to gene symbols
RNA-seq
updated 6 days ago by
Ram
44k • written 6 days ago by
ashkan
▴ 160
3
votes
2
replies
213
views
vg autoindex seems stuck after a week of running
vg
pangenome
22 hours ago by
StevieP
▴ 10
0
votes
3
replies
307
views
Kraken2 Custom Database non-deterministic results
Metagenomics
kraken2
updated 6 days ago by
colindaven
6.4k • written 8 days ago by
Bjorn
• 0
0
votes
1
reply
159
views
How to get 2 seurat objects into a DEseq
Seurat
DEseq
updated 6 days ago by
Ram
44k • written 7 days ago by
He11oJe11o
• 0
0
votes
0
replies
92
views
Rescaling normalized enrichment score (NES)
heatmap
6 days ago by
CTLong
▴ 110
0
votes
3
replies
224
views
Splitting query fasta file for Diamond Blastp make the process faster?
DIAMOND
4 days ago by
kmat
• 0
0
votes
1
reply
157
views
Mapping difference with BWA
variant-calling
samtools
bam
BWA
genomics
updated 6 days ago by
ATpoint
82k • written 7 days ago by
rj.rezwan
• 0
0
votes
0
replies
105
views
Kegg Pathways to Circos
Genomics
KEGG
Circos
7 days ago by
dlera.lozano
▴ 10
0
votes
0
replies
123
views
DIFFBIND boxplot results, p value not significant
DiffBind
ChIP-seq
6 days ago by
RD
▴ 10
3
votes
6
replies
358
views
Problem in getting geo file through GEOQUERY
geoquery
Geo
updated 6 days ago by
Ram
44k • written 7 days ago by
anasjamshed
▴ 120
0
votes
1
reply
189
views
Multi-ploid data in ANGSD and NGSadmix
ancestry
diploid
haploid
admixture
updated 7 days ago by
andersdetermig
▴ 20 • written 8 days ago by
Christopher
• 0
0
votes
2
replies
444
views
transanno liftvcf "Error: length of chromosome [chr] is not equal to length in chain file. Are you using correct reference?"
liftover
transanno
7 days ago by
ezz3
• 0
1
vote
10
replies
650
views
Add stats to the plot
R
6 days ago by
Ghada
• 0
0
votes
4
replies
250
views
Fewer sites in vcf than in reference genome despite Emit_All_Sites argument
GATK
UnifiedGenotyper
7 days ago by
shpak.max
▴ 50
2
votes
4
replies
284
views
Allele count of 2 for homoplasmic MT variants in VCF
Variant-Calling
GATK
VCF
6 days ago by
Arton
▴ 10
1
vote
3
replies
214
views
downloading chemical database from ChEMBL
ChEMBL
PyRMD
Virtual-Screening
updated 6 days ago by
GenoMax
142k • written 7 days ago by
s
• 0
0
votes
3
replies
196
views
Where are the illumina adapters on Trimmomatic take from?
rna-seq
trimmomatic
updated 7 days ago by
GenoMax
142k • written 7 days ago by
bioinfo
▴ 150
3
votes
2
replies
192
views
Multiplexing for pooled CRISPR screen sequencing
multiplex
CRISPR-screen
Illumina
6 days ago by
Tuấn Anh
• 0
2
votes
4
replies
1.2k
views
Is it possible to run CibersortX with a very small number of samples?
cibersortx
5 days ago by
Aspire
▴ 330
2
votes
4
replies
363
views
Functional enrichment analysis for unique gene IDs
RNA-SEQ
1 day ago by
Pegasus
▴ 100
11,722 results • Page
3 of 235
Recent Votes
Answer: DEG analysis with limma and contrast matrix using multiple Parkinson's cohorts i
Comment: DEG analysis with limma and contrast matrix using multiple Parkinson's cohorts i
Answer: help in changing Y scale in R
Answer: when I use htslib to write a bam. Error of "truncated file" shows by samtools
Survival analysis of TCGA patients integrating gene expression (RNASeq) data
Comment: I cannot download VG in any way
Why does WGCNA use weighted correlation instead of Pearson correlation?
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Comment: polygenic risk score
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▴ 20
Can't we calculate the prs of a single patient data with respect to GWAS data for predicting the risk for particular diseases?
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It is very common for studies like this to show no significant DE. Human studies like this where comparisons are made between diseases and …
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update. The error persists. With ValidateSamFile I get no error until i use MarkDuplicates. Then for the MarkDuplicates output I get: …
Comment: when I use htslib to write a bam. Error of "truncated file" shows by samtools
by
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Thanks very much.
Answer: help in changing Y scale in R
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4.2k
Hello @ab33b6d7 , Below is approximately the code block you provided, with a few additional lines added. Each of the new lines has > …
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Hi pubsurfted, I ran into the same issue using a reference transcriptome with HISAT2 from the Ensembl database. For others with similar e…
Comment: Intersection of multiple vcf files
by
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22k
isec is pretty awful for these set operations - especially since individual samples present alleles, not lines in a VCF file. If you can co…
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Maybe try to calculate min and max combined_min <- min(a_filtered$value, a_filtered_tv$value, na.rm = TRUE) combined_max <- max(a_…
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by
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82k
Use `+ylim(c(lower, upper))`. Either set manually, or query both `a_filtered` and `a_filtered_tv` for the minimum and maximum values that g…
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How come? If I have a pro-tumorigenic product, for example, wouldn't this comparison be valid?
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Thanks @Zhenyu Zhang for your response. I have just looked at the files you mentioned. Do you have any recommended package or code snippet …
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