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comments
0
votes
0
replies
124
views
Repeat expansion identification tools for long-read data
fragilex
repeatexpansion
long-read
fmr1
3 days ago by
adarsh_pp
▴ 40
2
votes
2
replies
184
views
Processing and calling SVs from PacBio data
PacBio
long-read
variant-calling
updated 16 days ago by
Ram
43k • written 16 days ago by
adarsh_pp
▴ 40
0
votes
0
replies
113
views
Long-read data for Alpha-Thalassemia
thalassemia
nanopore
lonngread
15 days ago by
adarsh_pp
▴ 40
1
vote
4
replies
766
views
gnomAD4.0 Hail Table Downloading
NGS
gnomAD
updated 5 weeks ago by
DBScan
▴ 300 • written 5 months ago by
adarsh_pp
▴ 40
0
votes
1
reply
180
views
Alignment tool of repeat expansion detection
STR
NGS
readexpansion
updated 5 weeks ago by
Jesse
▴ 740 • written 5 weeks ago by
adarsh_pp
▴ 40
0
votes
1
reply
295
views
Comment:
Comment: repeatseq compilation issues
5 weeks ago by
adarsh_pp
▴ 40
2
votes
4
replies
295
views
repeatseq compilation issues
NGS
Repeats
repeatseq
repeatexpansion
Genomics
updated 5 weeks ago by
Michael
54k • written 5 weeks ago by
adarsh_pp
▴ 40
2
votes
3
replies
383
views
Variant caller for Ion Torrent data
ThermoFisher
NGS
IonTorrent
Genomics
Variant-Calling
updated 5 weeks ago by
Brian Bushnell
20k • written 5 weeks ago by
adarsh_pp
▴ 40
0
votes
0
replies
383
views
Comment:
Comment: Variant caller for Ion Torrent data
5 weeks ago by
adarsh_pp
▴ 40
0
votes
1
reply
335
views
Variant calling from Mitochondrial Genome
Variant-Calling
NGS
Mitochondria
updated 16 days ago by
Ram
43k • written 3 months ago by
adarsh_pp
▴ 40
0
votes
1
reply
277
views
Variant missing in WGS sample
NGS
Variant-Calling
WGS
updated 4 months ago by
Ram
43k • written 4 months ago by
adarsh_pp
▴ 40
0
votes
1
reply
766
views
Comment:
Comment: gnomAD4.0 Hail Table Downloading
5 months ago by
adarsh_pp
▴ 40
0
votes
0
replies
998
views
Comment:
Comment: MMSplice score interpretation
5 months ago by
adarsh_pp
▴ 40
0
votes
1
reply
722
views
Comment:
Comment: BED files
6 months ago by
adarsh_pp
▴ 40
0
votes
6
replies
722
views
BED files
BED
NGS
Chromosomes
updated 6 months ago by
Ram
43k • written 6 months ago by
adarsh_pp
▴ 40
0
votes
3
replies
763
views
CNV calling
CNV
NGS
Variant-Calling
updated 7 months ago by
Zhenyu Zhang
★ 1.2k • written 15 months ago by
adarsh_pp
▴ 40
0
votes
3
replies
795
views
Comment:
Comment: Calculate the percentage of genomic region covered from the BED file.
8 months ago by
adarsh_pp
▴ 40
5
votes
6
replies
795
views
Calculate the percentage of genomic region covered from the BED file.
NGS
sequencing
genomics
exome
genes
updated 8 months ago by
rfran010
▴ 900 • written 8 months ago by
adarsh_pp
▴ 40
5
votes
2
replies
891
views
Variant caller for Nanopore sequencing data
Genomics
nanopore
sequencing
ont
long-read
updated 8 months ago by
colindaven
6.3k • written 8 months ago by
adarsh_pp
▴ 40
0
votes
0
replies
936
views
Comment:
Comment: GERP Score for variants
9 months ago by
adarsh_pp
▴ 40
1
vote
2
replies
936
views
GERP Score for variants
NGS
variants
prediction
pathogenic
9 months ago by
adarsh_pp
▴ 40
1
vote
0
replies
667
views
Comment:
Comment: GATK gCNV contig ploidy priors table
13 months ago by
adarsh_pp
▴ 40
2
votes
1
reply
667
views
GATK gCNV contig ploidy priors table
NGS
CNV
GATK.gCNV
Calling
Variant
13 months ago by
adarsh_pp
▴ 40
0
votes
3
replies
659
views
CNV Prediction Tools
NGS
Variant
CNV
Calling
updated 14 months ago by
Quentin M
▴ 60 • written 14 months ago by
adarsh_pp
▴ 40
1
vote
2
replies
903
views
BED file modification
BED
NGS
Chromosomes
updated 15 months ago by
Pierre Lindenbaum
161k • written 15 months ago by
adarsh_pp
▴ 40
5
votes
3
replies
862
views
Paired - end sequencing
NGS
Paired-end
Illumina
updated 15 months ago by
Prash
▴ 270 • written 15 months ago by
adarsh_pp
▴ 40
0
votes
1
reply
499
views
Annotating Cluster in scRNA-seq - Scanpy
cluster
cell
scRNAseq
annotation
single
updated 9 months ago by
dalibenam64
• 0 • written 22 months ago by
adarsh_pp
▴ 40
0
votes
0
replies
619
views
Comment:
Comment: Sanger Sequence Analysis
2.2 years ago by
adarsh_pp
▴ 40
5
votes
2
replies
619
views
Sanger Sequence Analysis
Sanger
2.2 years ago by
adarsh_pp
▴ 40
0
votes
0
replies
466
views
installing FinchTV or Chromas for Ubuntu OS.
Sequencing
finchtv
chromas
Sanger
updated 2.3 years ago by
Pierre Lindenbaum
161k • written 2.3 years ago by
adarsh_pp
▴ 40
0
votes
0
replies
976
views
Comment:
Comment: Somatic Variant Calling
2.4 years ago by
adarsh_pp
▴ 40
2
votes
3
replies
976
views
Somatic Variant Calling
BAM
NGS
Variants
Cancer
2.4 years ago by
adarsh_pp
▴ 40
0
votes
0
replies
404
views
Mapping Human Genome
NGS
Genome
Mapping
Reference
Human
2.4 years ago by
adarsh_pp
▴ 40
0
votes
1
reply
635
views
Tumor Mutation Burden
mutation
genome
tumour
Cancer
variants
updated 2.4 years ago by
Kevin Blighe
87k • written 2.4 years ago by
adarsh_pp
▴ 40
1
vote
2
replies
804
views
Variant Allele Frequency
Cancer
updated 2.6 years ago by
German.M.Demidov
★ 2.9k • written 2.6 years ago by
adarsh_pp
▴ 40
3
votes
3
replies
828
views
Germline Cancer Mutations
Cancer
updated 2.6 years ago by
benformatics
3.9k • written 2.6 years ago by
adarsh_pp
▴ 40
0
votes
1
reply
471
views
Microbial Genome Comparison with human genome
Microbiome
Genomics
Comparison
Genes
DNA
2.9 years ago by
adarsh_pp
▴ 40
0
votes
1
reply
658
views
Counting the number of species from NCBI Taxonomy browser
Taxonomy
NCBI
updated 3.2 years ago by
shenwei356
8.4k • written 3.2 years ago by
adarsh_pp
▴ 40
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