Showing: snpreset
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2
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WGS for mtDNA variation
mtdna sequencing snp assembly written 2.1 years ago by waqasnayab160 • updated 2 hours ago by Jeremy Leipzig18k
8
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2
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968
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9 follow
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Best tool for variant calling
genome alignment next-gen snp written 6 months ago by williamsbrian5064100 • updated 2 hours ago by claire0
3
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1
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92
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1
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92
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Automating to convert multiple fastq files into one fastq file
snp sequencing written 15 hours ago by zhou_12280 • updated 14 hours ago by genomax58k
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74
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829
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Report haplotype frequencies from a region within a phased vcf file
variation haplotype snp written 18 months ago by Krisr450 • updated 1 day ago by Biostar ♦♦ 20
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171
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107
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manhattan plot with Fst values
software error snp written 2 days ago by jaafari.omid0 • updated 2 days ago by RamRS19k
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121
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How can I find Variants position by GATK and Samtools
gatk samtools snp written 15 days ago by Mbillah100 • updated 3 days ago by Biostar ♦♦ 20
0
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105
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Lolliplot graph for mutations
R snp written 3 days ago by kavikrish19960
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54
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0
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Problems launching Lositan
next-gen outliers snp lositan written 3 days ago by lleipnitz0 • updated 3 days ago by h.mon21k
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46
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3
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Split VCF to individual scaffolds
genome assembly sequence snp vcf written 3.3 years ago by krp000120 • updated 3 days ago by zx87545.7k
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79
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0
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9
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2
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109
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6 follow
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Get Rs Number Based On Chromosome and Position
vcf rna-seq snp written 5 days ago by aiteteji10 • updated 4 days ago by Emily_Ensembl16k
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1
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54
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1
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Overlapped Variations Detecting
snp written 4 days ago by Mbillah100 • updated 4 days ago by Emily_Ensembl16k
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75
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Position error using write.plink
R snp plink snpstats write.plink written 4 days ago by ida.larsson20 • updated 4 days ago by zx87545.7k
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6
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16k
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24 follow
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Get rs number based on position
mysql snp ucsc written 7.5 years ago by Zach Stednick650 • updated 4 days ago by zx87545.7k
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92
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0
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1
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1
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86
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1
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How to make small subset of large genotyping dataset with plink?
snp written 4 days ago by kynnjo20 • updated 4 days ago by Inquisitive899540
1
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1
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88
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1
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Criteria for Overlapping SNPs
snp written 4 days ago by alexandramirandaaa0 • updated 4 days ago by WouterDeCoster34k
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210
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Overlapping SNPs in R
R snp homework written 6 days ago by alexandramirandaaa0 • updated 5 days ago by Jeremy Leipzig18k
1
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1
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508
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1
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is DANN capable of scoring insertion and deletion?
indel genome annotation snp non-coding written 20 months ago by fetus000020 • updated 5 days ago by Kevin Blighe32k
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61
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4
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147
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5 follow
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Take out One percent of the tops of numbers from the column in the table
R snp written 5 days ago by mostafarafiepour60 • updated 5 days ago by zx87545.7k
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45
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82
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0
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96
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SNP calling from BAM file
snp sequencing written 5 days ago by KXG0
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2
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464
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7 follow
2
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GWAS analysis tool
genome R snp written 4 months ago by arshad129240 • updated 5 days ago by breckuh20
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