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questions
2
votes
2
replies
325
views
Somatic Variant Calling from Nanopore Data
variant
somatic
calling
cancer
nanopore
updated 9 days ago by
GenoMax
145k • written 9 days ago by
adarsh_munna
▴ 50
0
votes
3
replies
336
views
Relative abundance of plasmid DNA content in each sample
Illumina
E.coli
WGS
15 days ago by
adarsh_munna
▴ 50
2
votes
1
reply
200
views
Assembly of chloroplast genome from plant WGS
Plant
assembly
chloroplast
Illumina
WGS
updated 17 days ago by
GenoMax
145k • written 17 days ago by
adarsh_munna
▴ 50
0
votes
3
replies
323
views
Demultiplexing Tool
NGS
Fastq
Demultiplexing
Thermo
updated 7 weeks ago by
rfran010
★ 1.3k • written 7 weeks ago by
adarsh_munna
▴ 50
0
votes
2
replies
421
views
Tools for chromosomal aneuploidy detection
human-genetics
aneuploidy
NGS
updated 3 months ago by
Ram
44k • written 3 months ago by
adarsh_munna
▴ 50
0
votes
0
replies
201
views
Repeat expansion identification tools for long-read data
fragilex
repeatexpansion
long-read
fmr1
4 months ago by
adarsh_munna
▴ 50
2
votes
2
replies
326
views
Processing and calling SVs from PacBio data
PacBio
long-read
variant-calling
updated 5 months ago by
Ram
44k • written 5 months ago by
adarsh_munna
▴ 50
0
votes
0
replies
179
views
Long-read data for Alpha-Thalassemia
thalassemia
nanopore
lonngread
5 months ago by
adarsh_munna
▴ 50
1
vote
4
replies
1.1k
views
gnomAD4.0 Hail Table Downloading
NGS
gnomAD
updated 5 months ago by
DBScan
▴ 420 • written 9 months ago by
adarsh_munna
▴ 50
0
votes
1
reply
275
views
Alignment tool of repeat expansion detection
STR
NGS
readexpansion
updated 5 months ago by
Jesse
▴ 780 • written 5 months ago by
adarsh_munna
▴ 50
2
votes
4
replies
444
views
repeatseq compilation issues
NGS
Repeats
repeatseq
repeatexpansion
Genomics
updated 5 months ago by
Michael
55k • written 5 months ago by
adarsh_munna
▴ 50
2
votes
3
replies
637
views
Variant caller for Ion Torrent data
ThermoFisher
NGS
IonTorrent
Genomics
Variant-Calling
updated 5 months ago by
Brian Bushnell
20k • written 5 months ago by
adarsh_munna
▴ 50
0
votes
1
reply
519
views
Variant calling from Mitochondrial Genome
Variant-Calling
NGS
Mitochondria
updated 5 months ago by
Ram
44k • written 7 months ago by
adarsh_munna
▴ 50
0
votes
1
reply
366
views
Variant missing in WGS sample
NGS
Variant-Calling
WGS
updated 8 months ago by
Ram
44k • written 8 months ago by
adarsh_munna
▴ 50
0
votes
6
replies
921
views
BED files
BED
NGS
Chromosomes
updated 10 months ago by
Ram
44k • written 11 months ago by
adarsh_munna
▴ 50
0
votes
3
replies
885
views
CNV calling
CNV
NGS
Variant-Calling
updated 11 months ago by
Zhenyu Zhang
★ 1.2k • written 19 months ago by
adarsh_munna
▴ 50
5
votes
6
replies
1.1k
views
Calculate the percentage of genomic region covered from the BED file.
NGS
sequencing
genomics
exome
genes
updated 13 months ago by
rfran010
★ 1.3k • written 13 months ago by
adarsh_munna
▴ 50
5
votes
2
replies
1.3k
views
Variant caller for Nanopore sequencing data
Genomics
nanopore
sequencing
ont
long-read
updated 13 months ago by
colindaven
6.7k • written 13 months ago by
adarsh_munna
▴ 50
1
vote
2
replies
1.2k
views
GERP Score for variants
NGS
variants
prediction
pathogenic
13 months ago by
adarsh_munna
▴ 50
2
votes
1
reply
792
views
GATK gCNV contig ploidy priors table
NGS
CNV
GATK.gCNV
Calling
Variant
18 months ago by
adarsh_munna
▴ 50
0
votes
3
replies
774
views
CNV Prediction Tools
NGS
Variant
CNV
Calling
updated 19 months ago by
Quentin M
▴ 60 • written 19 months ago by
adarsh_munna
▴ 50
1
vote
2
replies
1.0k
views
BED file modification
BED
NGS
Chromosomes
updated 19 months ago by
Pierre Lindenbaum
163k • written 19 months ago by
adarsh_munna
▴ 50
5
votes
3
replies
1.1k
views
Paired - end sequencing
NGS
Paired-end
Illumina
updated 20 months ago by
Prash
▴ 280 • written 20 months ago by
adarsh_munna
▴ 50
0
votes
1
reply
592
views
Annotating Cluster in scRNA-seq - Scanpy
cluster
cell
scRNAseq
annotation
single
updated 13 months ago by
dalibenam64
• 0 • written 2.2 years ago by
adarsh_munna
▴ 50
5
votes
2
replies
737
views
Sanger Sequence Analysis
Sanger
2.5 years ago by
adarsh_munna
▴ 50
0
votes
0
replies
546
views
installing FinchTV or Chromas for Ubuntu OS.
Sequencing
finchtv
chromas
Sanger
updated 2.7 years ago by
Pierre Lindenbaum
163k • written 2.7 years ago by
adarsh_munna
▴ 50
2
votes
3
replies
1.1k
views
Somatic Variant Calling
BAM
NGS
Variants
Cancer
2.7 years ago by
adarsh_munna
▴ 50
0
votes
0
replies
446
views
Mapping Human Genome
NGS
Genome
Mapping
Reference
Human
2.7 years ago by
adarsh_munna
▴ 50
0
votes
1
reply
689
views
Tumor Mutation Burden
mutation
genome
tumour
Cancer
variants
updated 2.8 years ago by
Kevin Blighe
88k • written 2.8 years ago by
adarsh_munna
▴ 50
1
vote
2
replies
898
views
Variant Allele Frequency
Cancer
updated 3.0 years ago by
German.M.Demidov
★ 2.9k • written 3.0 years ago by
adarsh_munna
▴ 50
3
votes
3
replies
933
views
Germline Cancer Mutations
Cancer
updated 3.0 years ago by
benformatics
4.0k • written 3.0 years ago by
adarsh_munna
▴ 50
0
votes
1
reply
510
views
Microbial Genome Comparison with human genome
Microbiome
Genomics
Comparison
Genes
DNA
3.3 years ago by
adarsh_munna
▴ 50
0
votes
1
reply
727
views
Counting the number of species from NCBI Taxonomy browser
Taxonomy
NCBI
updated 3.6 years ago by
shenwei356
8.6k • written 3.6 years ago by
adarsh_munna
▴ 50
33 results • Page
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