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0
votes
3
replies
249
views
Demultiplexing Tool
NGS Fastq Demultiplexing Thermo
updated 18 days ago by ★ 1.3k • written 19 days ago by ▴ 40
0
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2
replies
372
views
Tools for chromosomal aneuploidy detection
human-genetics aneuploidy NGS
updated 8 weeks ago by 44k • written 9 weeks ago by ▴ 40
0
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0
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186
views
Repeat expansion identification tools for long-read data
fragilex repeatexpansion long-read fmr1
3 months ago by adarsh_pp ▴ 40
2
votes
2
replies
292
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Processing and calling SVs from PacBio data
PacBio long-read variant-calling
updated 3 months ago by 44k • written 3 months ago by ▴ 40
0
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0
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161
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Long-read data for Alpha-Thalassemia
thalassemia nanopore lonngread
3 months ago by adarsh_pp ▴ 40
1
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4
replies
1.0k
views
gnomAD4.0 Hail Table Downloading
NGS gnomAD
updated 4 months ago by ▴ 380 • written 8 months ago by ▴ 40
0
votes
1
reply
248
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Alignment tool of repeat expansion detection
STR NGS readexpansion
updated 4 months ago by ▴ 770 • written 4 months ago by ▴ 40
0
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1
reply
401
views
Comment: Comment: repeatseq compilation issues
4 months ago by adarsh_pp ▴ 40
2
votes
4
replies
401
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repeatseq compilation issues
NGS Repeats repeatseq repeatexpansion Genomics
updated 4 months ago by 54k • written 4 months ago by ▴ 40
2
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3
replies
560
views
Variant caller for Ion Torrent data
ThermoFisher NGS IonTorrent Genomics Variant-Calling
updated 4 months ago by 20k • written 4 months ago by ▴ 40
0
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0
replies
560
views
Comment: Comment: Variant caller for Ion Torrent data
4 months ago by adarsh_pp ▴ 40
0
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1
reply
473
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Variant calling from Mitochondrial Genome
Variant-Calling NGS Mitochondria
updated 3 months ago by 44k • written 6 months ago by ▴ 40
0
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1
reply
342
views
Variant missing in WGS sample
NGS Variant-Calling WGS
updated 7 months ago by 44k • written 7 months ago by ▴ 40
0
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1
reply
1.0k
views
Comment: Comment: gnomAD4.0 Hail Table Downloading
8 months ago by adarsh_pp ▴ 40
0
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0
replies
1.1k
views
Comment: Comment: MMSplice score interpretation
9 months ago by adarsh_pp ▴ 40
0
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1
reply
866
views
Comment: Comment: BED files
9 months ago by adarsh_pp ▴ 40
0
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6
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866
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BED files
BED NGS Chromosomes
updated 9 months ago by 44k • written 10 months ago by ▴ 40
0
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3
replies
855
views
CNV calling
CNV NGS Variant-Calling
updated 10 months ago by ★ 1.2k • written 18 months ago by ▴ 40
0
votes
3
replies
982
views
Comment: Comment: Calculate the percentage of genomic region covered from the BED file.
12 months ago by adarsh_pp ▴ 40
5
votes
6
replies
982
views
Calculate the percentage of genomic region covered from the BED file.
NGS sequencing genomics exome genes
updated 12 months ago by ★ 1.3k • written 12 months ago by ▴ 40
5
votes
2
replies
1.2k
views
Variant caller for Nanopore sequencing data
Genomics nanopore sequencing ont long-read
updated 12 months ago by 6.5k • written 12 months ago by ▴ 40
0
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0
replies
1.1k
views
Comment: Comment: GERP Score for variants
12 months ago by adarsh_pp ▴ 40
1
vote
2
replies
1.1k
views
GERP Score for variants
NGS variants prediction pathogenic
12 months ago by adarsh_pp ▴ 40
1
vote
0
replies
761
views
Comment: Comment: GATK gCNV contig ploidy priors table
16 months ago by adarsh_pp ▴ 40
2
votes
1
reply
761
views
GATK gCNV contig ploidy priors table
NGS CNV GATK.gCNV Calling Variant
16 months ago by adarsh_pp ▴ 40
0
votes
3
replies
740
views
CNV Prediction Tools
NGS Variant CNV Calling
updated 17 months ago by ▴ 60 • written 17 months ago by ▴ 40
1
vote
2
replies
1.0k
views
BED file modification
BED NGS Chromosomes
updated 18 months ago by 163k • written 18 months ago by ▴ 40
5
votes
3
replies
998
views
Paired - end sequencing
NGS Paired-end Illumina
updated 18 months ago by ▴ 280 • written 19 months ago by ▴ 40
0
votes
1
reply
575
views
Annotating Cluster in scRNA-seq - Scanpy
cluster cell scRNAseq annotation single
updated 12 months ago by • 0 • written 2.1 years ago by ▴ 40
0
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0
replies
705
views
Comment: Comment: Sanger Sequence Analysis
2.4 years ago by adarsh_pp ▴ 40
5
votes
2
replies
705
views
Sanger Sequence Analysis
Sanger
2.4 years ago by adarsh_pp ▴ 40
0
votes
0
replies
526
views
installing FinchTV or Chromas for Ubuntu OS.
Sequencing finchtv chromas Sanger
updated 2.6 years ago by 163k • written 2.6 years ago by ▴ 40
0
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0
replies
1.1k
views
Comment: Comment: Somatic Variant Calling
2.6 years ago by adarsh_pp ▴ 40
2
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3
replies
1.1k
views
Somatic Variant Calling
BAM NGS Variants Cancer
2.6 years ago by adarsh_pp ▴ 40
0
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0
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433
views
Mapping Human Genome
NGS Genome Mapping Reference Human
2.6 years ago by adarsh_pp ▴ 40
0
votes
1
reply
672
views
Tumor Mutation Burden
mutation genome tumour Cancer variants
updated 2.7 years ago by 88k • written 2.7 years ago by ▴ 40
1
vote
2
replies
872
views
Variant Allele Frequency
Cancer
updated 2.9 years ago by ★ 2.9k • written 2.9 years ago by ▴ 40
3
votes
3
replies
895
views
Germline Cancer Mutations
Cancer
updated 2.9 years ago by 4.0k • written 2.9 years ago by ▴ 40
0
votes
1
reply
498
views
Microbial Genome Comparison with human genome
Microbiome Genomics Comparison Genes DNA
3.2 years ago by adarsh_pp ▴ 40
0
votes
1
reply
710
views
Counting the number of species from NCBI Taxonomy browser
Taxonomy NCBI
updated 3.5 years ago by 8.6k • written 3.5 years ago by ▴ 40
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