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− | <div style="font-size:162%; border:none; margin:0; padding:.1em; color:#000;">Abecasis Group Wiki</div> | + | {| style="width:100%; background:#fcfcfc; margin-top:1.2em; border:1px solid #ccc;" |
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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;">Abecasis Group Wiki</div> |
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| + | [[Image:AbecasisRetreat2016.jpg|700px|center|Group Photo 2016]] |
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− | [[Image:2009.08_Group_Retreat_Photo.jpg|400px|center|Group Photo]] | + | <!-- Below are old images from 2009 and 2014 Retreats --> |
| + | <!-- <br> [[Image:Abecasis2015Retreat.JPG|700px|center|Group Photo 2015]] --> |
| + | <!-- <br> [[Image:Abecasis2014Retreat.JPG|700px|center|Group Photo 2014]] --> |
| + | <!-- <br> [[Image:2009.08 Group Retreat Photo.jpg|center|400px|Group Photo]]--> |
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− | == Welcome! == | + | == Welcome! == |
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− | Welcome to our brand new wiki! | + | Welcome to our wiki! |
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− | If you would like to contribute, [[Special:UserLogin|log-in]] or [http://csgwiki.sph.umich.edu/index.php?title=Special:UserLogin&type=signup create an account]. We recommend using your e-mail address or Michigan uniqname as your user id. | + | If you would like to contribute, [[Special:UserLogin|log-in]] or [[Special:RequestAccount|request an account]]. We recommend using your e-mail address or Michigan uniqname as your user id. |
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− | For basic instructions, see [http://en.wikipedia.org/wiki/Wikipedia:Tutorial the Wikipedia Tutorial]. | + | For basic instructions, see [http://en.wikipedia.org/wiki/Wikipedia:Tutorial the Wikipedia Tutorial]. |
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− | == Sequence Analysis Tools == | + | == Sequence Analysis Tools == |
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− | We are developing several tools for the analysis of next generation sequence data. | + | We are developing [[Software|software tools]] for the analysis of next generation sequence data. |
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− | === [[Read Mapping]] ===
| + | These tools include: |
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− | [[Karma|Karma]] - Our fast short read aligner, which generates [[Mapping Quality Scores]] | + | #Variant Calling with [[GlfSingle]] and [[GlfMultiples]] |
| + | #Variant Calling and De Novo Mutation Detection in Families with [[Polymutt]] |
| + | #Variant Annotations using [[VcfCodingSnps]] |
| + | #Rare Variant Analysis using [[RvTests]] |
| + | #Rare Variant Association Analysis in family samples [[FamRvTest]] |
| + | #Quality control using [[C++ Executable: fastQValidator|FastQValidator]], [[VerifyBamID]], and [[BamValidator]] |
| + | #C++ APIs for sequence analsysis using [[C++ Library: libStatGen]] |
| + | #Meta-analysis of single variant or gene-level associations [[RAREMETAL-SOFTWARE]] |
| + | #Sequencing study design helper [[Rarefy]] |
| + | #Local ancestry inference (ancestry painting) using off-targeted sequence data [[SEQMIX]] |
| + | #Association Container Toolbox [[EPACTS]] |
| + | #Fast Genotype Imputation Tool : [[Minimac3]] |
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− | [[Karma-colorspace|Karma-ColorSpace]] - QUICKSTART on mapping color space reads | + | These tools and additional tools can be found on the [[Software]] page. |
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− | [[Examples|Examples]] - Sample command lines with discussion | + | We are developing Genome/Sequencing Processing Pipelines for anyone to use: [[GotCloud]] |
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− | === Variant Calling === | + | == High Level Tutorials == |
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− | [[glfSingle]] - Variant calling for a single, deeply sequenced individual
| + | Some high-level tutorials on the analysis of next generation sequence data: |
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− | [[glfTrio]] - Variant calling for a single, deeply sequenced nuclear family with two parents and one child | + | #[[Evaluating a Read Mapper on Simulated Data]] |
| + | #[[SNP Call Set Properties]] |
| + | #[[Generic Exome Analysis Plan]] |
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− | [[glfMultiples]] -- Variant calling for multiple, unrelated individuals
| + | == Projects == |
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− | === Variant Annotation ===
| + | [[NHLBI Informatics Resource|NHLBI Genome Sequencing Project]] |
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− | [[vcfCodingSnps]] -- Annotate coding variants in a VCF file. | + | [[SardiNIA]] - The SardiNIA longitudinal study of aging. |
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− | === Quality Control Utilities ===
| + | [[EMADS|Exome Meta-analysis of Drinking and Smoking (EMADS)]] |
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− | [[FastQ Validator]] -- Check that a FASTQ file conforms to specification. | + | [http://www.1000genomes.org The 1000 Genomes Project] |
− | [[FastQFile]] -- Read a FASTQ file sequence by sequence. Validating the sequence as it is read.
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− | [[BamIdentityCheck]] -- Check that mapped reads are consistent with known genotypes for each individual.
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− | === [[Links to Sequence Analysis Tools|Other Useful Links]] ===
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− | == Projects ==
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− | [[SardiNIA]] - The SardiNIA longitudinal study of aging.
| + | == Learn Genetics == |
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− | [[1000 Genomes Project Pilot 1 SNP Calling]] | + | Faculty in the group teach in a variety of formal and informal settings. [[Class Notes|Class notes]] and relevant discussion are archived here. |
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− | == Learn Genetics == | + | == General Resources == |
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− | Faculty in the group teach in a variety of formal and informal settings. [[Class Notes|Class notes]] and relevant discussion are archived here.
| + | *[[Computer How-Tos]] |
| + | </div> |