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1
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354
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Tool for identifying INDELs and Tandem duplication break points
svs tool written 18 months ago by swissman.howard97 • 0
2
votes
1
answer
1.3k
views
5 follow
1
answer
Merge CNVnator and Lumpy to find out copy number variants
svs cnvs written 2.1 years ago by Mbillah • 120 • updated 20 months ago by Mant • 10
0
votes
0
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409
views
0
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Germline and somatic model, which one is preferred to call SVs fish male and female population
genome svs written 2.2 years ago by bioming • 0 • updated 2.2 years ago by WouterDeCoster ♦ 45k
0
votes
1
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469
views
1
answer
News: Registration deadline: Comparative genomics
news svs snp written 2.4 years ago by carlopecoraro2 • 1.9k
3
votes
0
answers
2.0k
views
7 follow
0
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Detecting Structural variants in sequencing data
structural variants calling svs sequencing written 3.6 years ago by Glen • 20 • updated 3.2 years ago by Biostar ♦♦ 20
0
votes
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721
views
0
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Running Pindel individually per sample rather than running everything as it expects
ngs svs pindel written 3.6 years ago by mehmetgoktay1989 • 0
3
votes
1
answer
2.5k
views
1
answer
Anyone used BAMSurgeon to spike in 1KB insertions/deletions?
genome bam bamsurgeon svs written 5.3 years ago by sichan • 90 • updated 3.9 years ago by lzy • 20
0
votes
0
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811
views
0
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Software SVS for DNA-seq
dna-seq cattle svs rna-seq written 4.3 years ago by gabriela.ribeiro.br • 10 • updated 4.3 years ago by GenoMax ♦ 94k
2
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0
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1.2k
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0
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Representative set for normal structural variation
genome structural variants svs dbvar dgv written 6.3 years ago by dmyersturnbull • 90
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