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, 12:45, 1 May 2012
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| [[Category:Software]] | | [[Category:Software]] |
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| + | | style="width:100%; text-align:center; white-space:nowrap; color:#000;" | |
| + | <div style="font-size:162%; border:none; margin:0; padding:.1em; color:#000;">This tool has been DEPRECATED, and replaced by [[Polymutt]]</div> |
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| '''glfTrio''' is a [[GLF]]-based variant caller for next-generation sequencing data. It takes three [[GLF]] format genotype likelihood files as input and generates a [[VCF]]-format set of variant calls as output. | | '''glfTrio''' is a [[GLF]]-based variant caller for next-generation sequencing data. It takes three [[GLF]] format genotype likelihood files as input and generates a [[VCF]]-format set of variant calls as output. |
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| --xStop ''sexChromosomeEnd'' End of the non-pseudo-autosomal portion of the X (154,584,237 bp in build 36) | | --xStop ''sexChromosomeEnd'' End of the non-pseudo-autosomal portion of the X (154,584,237 bp in build 36) |
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− | For NCBI genome build 36, you should use the settings --xChr X --xStart 2709521 --xStop 154584237 | + | For NCBI genome build 36, you should use the settings <code>--xChr X --xStart 2709521 --xStop 154584237</code> |
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− | For NCBI genome build 37, you should use the settings --xChr X --xStart 2699520 --xStop 154931044 | + | For NCBI genome build 37, you should use the settings <code>--xChr X --xStart 2699520 --xStop 154931044</code> |
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| == Model for Variant Calling == | | == Model for Variant Calling == |