ANGSD: Analysis of next generation Sequencing Data

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Genotype Likelihoods: Difference between revisions

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(Created page with "==Genotype likelihoods from alignments== ===Kim et al.=== Citation Citation ===Samtools=== ===GATK===")
 
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==Genotype likelihoods from alignments==
==Genotype likelihoods from alignments==
 
; -GL [int]
If your input is sequencing file you can estimate genotype likelhoods from the mapped reads. Four different methods are available.
===soapSNP===
-GL 0
===Samtools===
-GL 1
===GATK===
-GL 2
===Kim et al.===
===Kim et al.===
 
-GL 3
[[Kim10|Citation]] [[Kim11|Citation]]
[[Kim10|Citation]] [[Kim11|Citation]]
===Samtools===
===GATK===

Revision as of 20:05, 18 June 2012

Genotype likelihoods from alignments

-GL [int]

If your input is sequencing file you can estimate genotype likelhoods from the mapped reads. Four different methods are available.

soapSNP

-GL 0

Samtools

-GL 1

GATK

-GL 2

Kim et al.

-GL 3 Citation Citation