From Genome Analysis Wiki
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, 18:59, 14 November 2009
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| Welcome to our brand new wiki! | | Welcome to our brand new wiki! |
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− | For basic instructions, see [[basic instructions]]. | + | For basic instructions, see [[http://en.wikipedia.org/wiki/Wikipedia:Tutorial the Wikipedia Tutorial]]. |
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− | We suggest using your uniqname as your login ID here. Please DO NOT use your umich kerberos password here.
| + | == Sequence Analysis Tools == |
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− | == What Is Available ==
| + | We are developing several tools for the analysis of next generation sequence data. |
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− | You have come to the right place for documentation of:
| + | === Read Mapping === |
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| [[Karma|Karma]] - Our fast short read aligner | | [[Karma|Karma]] - Our fast short read aligner |
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| [[Karma-colorspace|Karma-ColorSpace]] - QUICKSTART on mapping color space reads | | [[Karma-colorspace|Karma-ColorSpace]] - QUICKSTART on mapping color space reads |
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| + | === Variant Calling === |
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| + | [[glfSingle]] - Variant calling for a single, deeply sequenced individual |
| + | [[glfTrio]] - Variant calling for a single, deeply sequence nuclear family with two parents and one child |
| + | [[glfMultiples]] -- Variant calling for multiple, unrelated individuals |