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questions
2
votes
1
reply
250
views
SRA-Submission query (BioProject)
NGS
Raw
SRA
data
updated 9 days ago by
GenoMax
148k • written 9 days ago by
adarsh_munna
▴ 50
1
vote
1
reply
296
views
SNP Density plot with custom genome using karyoploteR
NGS
SNP
R
updated 10 weeks ago by
zx8754
12k • written 10 weeks ago by
adarsh_munna
▴ 50
0
votes
2
replies
312
views
Tools for assembling Plasmid Genome
Illumina
Plasmid
E.coli
Assembly
11 weeks ago by
adarsh_munna
▴ 50
2
votes
2
replies
441
views
Somatic Variant Calling from Nanopore Data
variant
somatic
calling
cancer
nanopore
updated 3 months ago by
GenoMax
148k • written 3 months ago by
adarsh_munna
▴ 50
0
votes
3
replies
439
views
Relative abundance of plasmid DNA content in each sample
Illumina
E.coli
WGS
3 months ago by
adarsh_munna
▴ 50
2
votes
1
reply
263
views
Assembly of chloroplast genome from plant WGS
Plant
assembly
chloroplast
Illumina
WGS
updated 4 months ago by
GenoMax
148k • written 4 months ago by
adarsh_munna
▴ 50
0
votes
3
replies
491
views
Demultiplexing Tool
NGS
Fastq
Demultiplexing
Thermo
updated 5 months ago by
rfran010
★ 1.3k • written 5 months ago by
adarsh_munna
▴ 50
0
votes
2
replies
536
views
Tools for chromosomal aneuploidy detection
human-genetics
aneuploidy
NGS
updated 6 months ago by
Ram
44k • written 6 months ago by
adarsh_munna
▴ 50
0
votes
0
replies
228
views
Repeat expansion identification tools for long-read data
fragilex
repeatexpansion
long-read
fmr1
8 months ago by
adarsh_munna
▴ 50
2
votes
2
replies
409
views
Processing and calling SVs from PacBio data
PacBio
long-read
variant-calling
updated 8 months ago by
Ram
44k • written 8 months ago by
adarsh_munna
▴ 50
0
votes
0
replies
215
views
Long-read data for Alpha-Thalassemia
thalassemia
nanopore
lonngread
8 months ago by
adarsh_munna
▴ 50
1
vote
4
replies
1.3k
views
gnomAD4.0 Hail Table Downloading
NGS
gnomAD
updated 9 months ago by
DBScan
▴ 450 • written 13 months ago by
adarsh_munna
▴ 50
0
votes
1
reply
331
views
Alignment tool of repeat expansion detection
STR
NGS
readexpansion
updated 9 months ago by
Jesse
▴ 850 • written 9 months ago by
adarsh_munna
▴ 50
2
votes
4
replies
528
views
repeatseq compilation issues
NGS
Repeats
repeatseq
repeatexpansion
Genomics
updated 9 months ago by
Michael
55k • written 9 months ago by
adarsh_munna
▴ 50
2
votes
3
replies
818
views
Variant caller for Ion Torrent data
ThermoFisher
NGS
IonTorrent
Genomics
Variant-Calling
updated 9 months ago by
Brian Bushnell
20k • written 9 months ago by
adarsh_munna
▴ 50
0
votes
1
reply
628
views
Variant calling from Mitochondrial Genome
Variant-Calling
NGS
Mitochondria
updated 8 months ago by
Ram
44k • written 11 months ago by
adarsh_munna
▴ 50
0
votes
1
reply
417
views
Variant missing in WGS sample
NGS
Variant-Calling
WGS
updated 12 months ago by
Ram
44k • written 12 months ago by
adarsh_munna
▴ 50
0
votes
6
replies
1.0k
views
BED files
BED
NGS
Chromosomes
updated 14 months ago by
Ram
44k • written 14 months ago by
adarsh_munna
▴ 50
0
votes
3
replies
964
views
CNV calling
CNV
NGS
Variant-Calling
updated 14 months ago by
Zhenyu Zhang
★ 1.2k • written 23 months ago by
adarsh_munna
▴ 50
5
votes
6
replies
1.2k
views
Calculate the percentage of genomic region covered from the BED file.
NGS
sequencing
genomics
exome
genes
updated 16 months ago by
rfran010
★ 1.3k • written 16 months ago by
adarsh_munna
▴ 50
5
votes
2
replies
1.7k
views
Variant caller for Nanopore sequencing data
Genomics
nanopore
sequencing
ont
long-read
updated 16 months ago by
colindaven
7.0k • written 16 months ago by
adarsh_munna
▴ 50
1
vote
2
replies
1.3k
views
GERP Score for variants
NGS
variants
prediction
pathogenic
17 months ago by
adarsh_munna
▴ 50
2
votes
1
reply
846
views
GATK gCNV contig ploidy priors table
NGS
CNV
GATK.gCNV
Calling
Variant
21 months ago by
adarsh_munna
▴ 50
0
votes
3
replies
838
views
CNV Prediction Tools
NGS
Variant
CNV
Calling
updated 22 months ago by
Quentin M
▴ 60 • written 22 months ago by
adarsh_munna
▴ 50
1
vote
2
replies
1.1k
views
BED file modification
BED
NGS
Chromosomes
updated 23 months ago by
Pierre Lindenbaum
164k • written 23 months ago by
adarsh_munna
▴ 50
5
votes
3
replies
1.2k
views
Paired - end sequencing
NGS
Paired-end
Illumina
updated 23 months ago by
Prash
▴ 280 • written 23 months ago by
adarsh_munna
▴ 50
0
votes
1
reply
631
views
Annotating Cluster in scRNA-seq - Scanpy
cluster
cell
scRNAseq
annotation
single
updated 17 months ago by
dalibenam64
• 0 • written 2.5 years ago by
adarsh_munna
▴ 50
5
votes
2
replies
790
views
Sanger Sequence Analysis
Sanger
2.8 years ago by
adarsh_munna
▴ 50
0
votes
0
replies
587
views
installing FinchTV or Chromas for Ubuntu OS.
Sequencing
finchtv
chromas
Sanger
updated 3.0 years ago by
Pierre Lindenbaum
164k • written 3.0 years ago by
adarsh_munna
▴ 50
2
votes
3
replies
1.2k
views
Somatic Variant Calling
BAM
NGS
Variants
Cancer
3.0 years ago by
adarsh_munna
▴ 50
0
votes
0
replies
468
views
Mapping Human Genome
NGS
Genome
Mapping
Reference
Human
3.0 years ago by
adarsh_munna
▴ 50
0
votes
1
reply
716
views
Tumor Mutation Burden
mutation
genome
tumour
Cancer
variants
updated 3.1 years ago by
Kevin Blighe
88k • written 3.1 years ago by
adarsh_munna
▴ 50
1
vote
2
replies
941
views
Variant Allele Frequency
Cancer
updated 3.3 years ago by
German.M.Demidov
★ 2.9k • written 3.3 years ago by
adarsh_munna
▴ 50
3
votes
3
replies
993
views
Germline Cancer Mutations
Cancer
updated 3.3 years ago by
benformatics
4.1k • written 3.3 years ago by
adarsh_munna
▴ 50
0
votes
1
reply
528
views
Microbial Genome Comparison with human genome
Microbiome
Genomics
Comparison
Genes
DNA
3.6 years ago by
adarsh_munna
▴ 50
0
votes
1
reply
765
views
Counting the number of species from NCBI Taxonomy browser
Taxonomy
NCBI
updated 3.8 years ago by
shenwei356
8.7k • written 3.8 years ago by
adarsh_munna
▴ 50
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