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<prev • 46 results • page 1 of 2 • next >
2
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669
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Nanopore SNP and indels calling tool
snps indels tools calling nanopore written 7 months ago by tarek.mohamed • 240 • updated 12 weeks ago by WouterDeCoster ♦ 36k
0
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1
answer
267
views
1
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GATK Panel Of Normals (PoN)
gatk beta calling variant written 3 months ago by b.d237 • 40
0
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0
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233
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0
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SNP/Mbp rate weird, any known bias/artifact?
mbp calling variant snp bias written 10 months ago by Macspider • 2.7k
2
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1
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574
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1
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How to detect False positive variant in repeat region ?
vcf calling bam written 11 months ago by istdasklar • 0 • updated 11 months ago by Kevin Blighe ♦ 37k
3
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3
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6.2k
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5 follow
3
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How To Get Consensus Sequence Including Variant From A Vcf File For Several Individuals...?
vcf consensus calling variant gatk written 6.4 years ago by Bioch'Ti • 1000 • updated 12 months ago by boczniak767 • 620
0
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1
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914
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1
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mpileup for PacBio reads
quiver calling pacbio mpileup variants written 22 months ago by Biomonika (Noolean) ♦ 3.0k • updated 14 months ago by tjduncan • 230
3
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0
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1.2k
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7 follow
0
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Detecting Structural variants in sequencing data
structural variants calling svs sequencing written 20 months ago by Glen • 20 • updated 15 months ago by Biostar ♦♦ 20
1
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1
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644
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1
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VCF Indel line structure: what is actually reported?
indel vcf calling variant snp written 22 months ago by Macspider • 2.7k • updated 20 months ago by Biostar ♦♦ 20
0
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0
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548
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0
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Getting SNPs that are the complementary base of the reference
calling allele variant snp alternative written 23 months ago by Macspider • 2.7k
5
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1
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637
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1
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VCF Format INFO field: why do some keys in it not appear in the documentation?
vcf format calling snp variants written 2.2 years ago by Macspider • 2.7k • updated 2.2 years ago by Pierre Lindenbaum ♦ 117k
4
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1
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733
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1
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Variant Calling problem - find alternate heterozygous
vcf calling heterozygous variant written 2.3 years ago by Paul • 1.3k • updated 2.3 years ago by Zaag • 670
4
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0
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1.3k
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0
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INDEL and point mutation at same position in VCF
vcf indels calling snps alignment written 3.7 years ago by simono101 • 20 • updated 2.5 years ago by Biostar ♦♦ 20
2
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1
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1.3k
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1
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filtering pindel results
indel calling rearrangement filtering pindel written 2.6 years ago by Tootiki • 40
27
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6
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2.0k
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6
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Does anyone use Python for variant calling?
python ngs calling variant snp written 2.7 years ago by mhmtgenc85 • 30 • updated 2.7 years ago by Zaag • 670
9
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5
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3.3k
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5
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SNP calling pipeline - testing different programs
snp calling mapping filtering written 3.8 years ago by Eric Normandeau ♦ 10k • updated 2.9 years ago by alexisdereeper • 30
5
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1
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4.1k
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1
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Snp Calling With Bcftools Using Pileup File Format Instead Of Bcf
calling bcftools snp written 5.6 years ago by Justin • 440 • updated 4.1 years ago by Biostar ♦♦ 20
4
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1
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5.1k
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7 follow
1
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Filtering Variant Calls Based On Genotype Quality
calling variant filtering written 6.3 years ago by Kssr • 110 • updated 4.2 years ago by Biostar ♦♦ 20
7
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2
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5.3k
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8 follow
2
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Haplotype Calling
haplotype calling 454 sequencing written 6.5 years ago by Empyrean • 160 • updated 4.3 years ago by Biostar ♦♦ 20
1
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3
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2.3k
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3
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How Can I Get The Field Of Ac Key-Value Pair In The Info Column In Vcf File?
vcf calling frequency allele variant written 5.0 years ago by cli2 • 0
10
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1
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5.9k
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9 follow
1
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Tetraploid Snp Calling & Snp Filtering
quality calling samtools snp written 5.0 years ago by pavenhuizen • 70 • updated 5.0 years ago by Adrian Pelin • 2.2k
2
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1
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1.4k
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1
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How To Deal With Wild-Type Versus No-Calls In Exomes?
exome calling variant human written 5.0 years ago by Chris Cole • 680 • updated 5.0 years ago by Daniel Swan ♦ 13k
3
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1
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2.2k
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1
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Fasta File For Exomedepth And Cnv Calling
exon R ngs calling cnv exome written 5.1 years ago by Jimbou • 670
0
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1
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1.9k
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1
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Realignertargetcreator --- Arrayindexoutofboundsexception
gatk next-gen calling variant written 6.6 years ago by sandeep.deverasetty • 60 • updated 5.2 years ago by Biostar ♦♦ 20
4
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1
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3.6k
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6 follow
1
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How To Prepare Gatk .Vcf Files Output For Annovar ?
vcf gatk calling variant annovar written 5.6 years ago by newDNASeqer • 630 • updated 5.6 years ago by Malachi Griffith ♦ 17k
7
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2
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3.8k
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7 follow
2
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Paper Or Detailed Tutorial For Dna Variant Calling Pipeline? Need Help To Start
variant calling pipeline dna written 5.6 years ago by newDNASeqer • 630 • updated 5.6 years ago by rob234king • 560
13
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4
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7.4k
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9 follow
4
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How To Interprete/Display .Vcf Data File?
vcf calling variant written 5.6 years ago by newDNASeqer • 630 • updated 5.6 years ago by alaincoletta • 110
1
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1
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8.6k
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5 follow
1
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Paired-End Reads Alignment For Variant Calling ?
calling gatk paired-end picard variant written 5.6 years ago by newDNASeqer • 630 • updated 5.6 years ago by Ashutosh Pandey ♦ 11k
6
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2
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3.0k
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2
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Chip Seq Analysis Using Macs At A Pvalue Of 1E-2 Then Interesecting To Call "True Peaks"
macs calling peak-calling written 5.6 years ago by jhrf • 10 • updated 5.6 years ago by alessandro.riccombeni • 20
1
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1
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2.0k
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1
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Does Anybody Know Which Gatk Walkers Are Positively Affected By Pedigree Information?
gatk calling written 5.8 years ago by Matt Miossec • 320 • updated 5.8 years ago by vdauwera • 890
0
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1.4k
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0
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How To Call Cnvs From Raw Intensities
array illumina calling written 6.0 years ago by elengss • 0 • updated 6.0 years ago by Istvan Albert ♦♦ 79k
<prev • 46 results • page 1 of 2 • next >
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