<div dir="ltr"><div class="gmail_default" style="font-family:verdana,sans-serif;font-size:small">Prezados(as)</div><div class="gmail_default" style="font-family:verdana,sans-serif;font-size:small"><br></div><div class="gmail_default" style="font-family:verdana,sans-serif;font-size:small"><div class="gmail_default" style="font-size:small;color:rgb(34,34,34);font-style:normal;font-variant-ligatures:normal;font-variant-caps:normal;font-weight:400;letter-spacing:normal;text-align:start;text-indent:0px;text-transform:none;white-space:normal;word-spacing:0px;text-decoration-style:initial;text-decoration-color:initial;font-family:verdana,sans-serif">Estamos de volta com nossos seminários em Análise de Dados em Alta Dimensão ( <AD,AD> ) </div><div class="gmail_default" style="font-size:small;color:rgb(34,34,34);font-style:normal;font-variant-ligatures:normal;font-variant-caps:normal;font-weight:400;letter-spacing:normal;text-align:start;text-indent:0px;text-transform:none;white-space:normal;word-spacing:0px;text-decoration-style:initial;text-decoration-color:initial;font-family:verdana,sans-serif"><br></div><div class="gmail_default" style="font-size:small;color:rgb(34,34,34);font-style:normal;font-variant-ligatures:normal;font-variant-caps:normal;font-weight:400;letter-spacing:normal;text-align:start;text-indent:0px;text-transform:none;white-space:normal;word-spacing:0px;text-decoration-style:initial;text-decoration-color:initial;font-family:verdana,sans-serif">Quarta-feira, as 13hs, sala 221.</div><div class="gmail_default" style="font-size:small;color:rgb(34,34,34);font-style:normal;font-variant-ligatures:normal;font-variant-caps:normal;font-weight:400;letter-spacing:normal;text-align:start;text-indent:0px;text-transform:none;white-space:normal;word-spacing:0px;text-decoration-style:initial;text-decoration-color:initial;font-family:verdana,sans-serif">Nesta semana teremos</div><div class="gmail_default" style="font-size:small;color:rgb(34,34,34);font-style:normal;font-variant-ligatures:normal;font-variant-caps:normal;font-weight:400;letter-spacing:normal;text-align:start;text-indent:0px;text-transform:none;white-space:normal;word-spacing:0px;text-decoration-style:initial;text-decoration-color:initial;font-family:verdana,sans-serif"><br></div><div class="gmail_default" style="font-size:small;color:rgb(34,34,34);font-style:normal;font-variant-ligatures:normal;font-variant-caps:normal;font-weight:400;letter-spacing:normal;text-align:start;text-indent:0px;text-transform:none;white-space:normal;word-spacing:0px;text-decoration-style:initial;text-decoration-color:initial;font-family:verdana,sans-serif"><span></span><p class="gmail-p1" style="margin:0px;text-align:center;font-style:normal;font-variant:normal;font-weight:normal;font-stretch:normal;font-size:12px;line-height:normal;font-family:"Trebuchet MS";color:rgb(0,0,0)"><span class="gmail-s1" style="font-kerning:none"><b>Using SNP Array Data for Genotype Inference</b></span></p><p class="gmail-p1" style="margin:0px;text-align:center;font-style:normal;font-variant:normal;font-weight:normal;font-stretch:normal;font-size:12px;line-height:normal;font-family:"Trebuchet MS";color:rgb(0,0,0)"><span class="gmail-s1" style="font-kerning:none"><i>Benilton S Carvalho</i></span></p><p class="gmail-p2" style="margin:0px;text-align:center;font-style:normal;font-variant:normal;font-weight:normal;font-stretch:normal;font-size:12px;line-height:normal;font-family:"Trebuchet MS";color:rgb(0,0,0);min-height:14px"><span class="gmail-s1" style="font-kerning:none"></span><br></p><p class="gmail-p3" style="margin:0px;text-align:justify;font-style:normal;font-variant:normal;font-weight:normal;font-stretch:normal;font-size:12px;line-height:normal;font-family:"Trebuchet MS";color:rgb(0,0,0);min-height:14px"><span class="gmail-s1" style="font-kerning:none"></span><br></p><p class="gmail-p4" style="margin:0px;text-align:justify;font-style:normal;font-variant:normal;font-weight:normal;font-stretch:normal;font-size:12px;line-height:normal;font-family:"Trebuchet MS";color:rgb(0,0,0)"><span class="gmail-s1" style="font-kerning:none">With the development of Precision Medicine, i.e., the use of personal genomic information to further improve diagnostics and treatment, data analysts face more frequently the necessity of dealing with larger volumes of data. One common task in this context is genotyping, where the investigator uses data on allele-specific relative abundances to identify the subject’s version of the genome at a particular position. This position that is likely to host “different versions of the genome” (genotype) for each subject is called Single Nucleotide Polymorphism, SNP. SNPs are observed at every 100-300 nucleotides, adding up to possibly 30 million markers. There are different technologies that provide data for one to infer genotypes starting from a DNA sample. The two most popular technologies are microarrays and next-generation sequencing. In this talk, we will discuss CRLMM, a genotyping methodology developed from SNP microarrays, which has been used successfully in several studies, including the BRAINN RIDC.</span></p></div><br></div><br clear="all"><div><br></div>-- <br><div class="gmail_signature" data-smartmail="gmail_signature"><div dir="ltr"><div><div>Ronaldo Dias</div>Professor<div>Dept. of Statistics-IMECC, UNICAMP</div><div><a href="http://www.ime.unicamp.br/~dias" target="_blank">www.ime.unicamp.br/~dias</a></div><div><br></div></div></div></div>
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