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<p class="MsoNormal" style="margin-bottom:9.6pt;background:white"><b><span style="font-size:12.0pt;font-family:"Arial",sans-serif;color:#232642;mso-fareast-language:EN-GB">Computational postdoctoral fellow in medical genomics<o:p></o:p></span></b></p>
<p class="MsoNormal"><span style="font-size:13.0pt"><a href="https://urldefense.proofpoint.com/v2/url?u=https-3A__eur03.safelinks.protection.outlook.com_-3Furl-3Dhttps-253A-252F-252Fjobs.sanger.ac.uk-252Fvacancy-252Fcomputational-2Dpostdoctoral-2Dfellow-2Din-2Dmedical-2Dgenomics-2D480295.html-26data-3D04-257C01-257Csegeg-2540mailman.kcl.ac.uk-257Cf9e6a91fac694ef1d12508da10bf3840-257C8370cf1416f34c16b83c724071654356-257C0-257C0-257C637840710716036121-257CUnknown-257CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0-253D-257C3000-26sdata-3DnLosXHdVg-252BfDX3pHYC00iwWhcKqIsEybLhaymsc0smQ-253D-26reserved-3D0&d=DwMGaQ&c=D7ByGjS34AllFgecYw0iC6Zq7qlm8uclZFI0SqQnqBo&r=tf9MksA2A9wnBTXR1i5jSZxGLz7bbhC51Hd7GnvhmqQ&m=Zh0t62ojFUongfqJ4FhGAsrixvBTOfcuoLpeI-5pkrRBU8Sz5Y7sd2r2ctkcaYi8&s=buCk0eH1UBm70aTDqw88OV_Z-F7qwvZyXwcCOIwginU&e=">https://jobs.sanger.ac.uk/vacancy/computational-postdoctoral-fellow-in-medical-genomics-480295.html
 [eur03.safelinks.protection.outlook.com]</a><o:p></o:p></span></p>
<p style="background:white"><span style="font-size:12.0pt;font-family:"Helvetica Neue LT W05 55 Roman";color:#232642">We are seeking a highly motivated postdoctoral fellow to join the <a href="https://urldefense.proofpoint.com/v2/url?u=https-3A__eur03.safelinks.protection.outlook.com_-3Furl-3Dhttps-253A-252F-252Fwww.sanger.ac.uk-252Fgroup-252Fmartin-2Dgroup-252F-26data-3D04-257C01-257Csegeg-2540mailman.kcl.ac.uk-257Cf9e6a91fac694ef1d12508da10bf3840-257C8370cf1416f34c16b83c724071654356-257C0-257C0-257C637840710716036121-257CUnknown-257CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0-253D-257C3000-26sdata-3D-252F1jn-252FIwgC8fkX6UD6-252BzjtVZrrF92CldK8y22k7otnT8-253D-26reserved-3D0&d=DwMGaQ&c=D7ByGjS34AllFgecYw0iC6Zq7qlm8uclZFI0SqQnqBo&r=tf9MksA2A9wnBTXR1i5jSZxGLz7bbhC51Hd7GnvhmqQ&m=Zh0t62ojFUongfqJ4FhGAsrixvBTOfcuoLpeI-5pkrRBU8Sz5Y7sd2r2ctkcaYi8&s=PM6h0VOKsiPg18YshjcNWgOEcW567uiVJgHJM8cO8CI&e=" target="_blank" title="* this link opens in a new window/tab"><span style="color:#597FBA">Martin
 group</span> [eur03.safelinks.protection.outlook.com]</a> at the Wellcome Sanger Institute, to work on the </span><span style="font-size:12.0pt;font-family:"Helvetica Neue LT W05_75 Bold";color:#232642">genetics of autism and developmental disorders</span><span style="font-size:12.0pt;font-family:"Helvetica Neue LT W05 55 Roman";color:#232642">.<o:p></o:p></span></p>
<p style="background:white;box-sizing: inherit;margin-top:1rem;margin-bottom:1rem;font-variant-ligatures: normal;font-variant-caps: normal;orphans: 2;text-align:start;widows: 2;-webkit-text-stroke-width: 0px;text-decoration-thickness: initial;text-decoration-style: initial;text-decoration-color: initial;word-spacing:0px">
<span style="font-size:12.0pt;font-family:"Helvetica Neue LT W05 55 Roman";color:#232642"> The group investigates the genetic basis of rare and common diseases, as well as population genetic processes that influence the distribution of genetic variation. We
 currently have projects in the following areas:<o:p></o:p></span></p>
<ul type="disc">
<li class="MsoNormal" style="color:#232642;mso-margin-top-alt:auto;mso-margin-bottom-alt:auto;mso-list:l1 level1 lfo3;background:white;box-sizing: inherit;font-size:1rem;padding-left:0.35rem">
<span style="font-size:12.0pt;font-family:"Helvetica Neue LT W05 55 Roman"">The role of both rare and common variants in rare disorders, using data from the <a href="https://urldefense.proofpoint.com/v2/url?u=https-3A__eur03.safelinks.protection.outlook.com_-3Furl-3Dhttps-253A-252F-252Fwww.sanger.ac.uk-252Fcollaboration-252Fdeciphering-2Ddevelopmental-2Ddisorders-2Dddd-252F-26data-3D04-257C01-257Csegeg-2540mailman.kcl.ac.uk-257Cf9e6a91fac694ef1d12508da10bf3840-257C8370cf1416f34c16b83c724071654356-257C0-257C0-257C637840710716036121-257CUnknown-257CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0-253D-257C3000-26sdata-3DPRYkb-252Bt6V136T3l4yoEvotaPH-252BBrINWKAsiYa-252Bos3pU-253D-26reserved-3D0&d=DwMGaQ&c=D7ByGjS34AllFgecYw0iC6Zq7qlm8uclZFI0SqQnqBo&r=tf9MksA2A9wnBTXR1i5jSZxGLz7bbhC51Hd7GnvhmqQ&m=Zh0t62ojFUongfqJ4FhGAsrixvBTOfcuoLpeI-5pkrRBU8Sz5Y7sd2r2ctkcaYi8&s=hL7gdYN77_mcZjmPyj9BMFN2U3TYKuLMdRyw_r5nAlA&e=" target="_blank" title="* this link opens in a new window/tab"><span style="color:#597FBA">Deciphering
 Developmental Disorders</span> [eur03.safelinks.protection.outlook.com]</a> study and the Genomics England <a href="https://urldefense.proofpoint.com/v2/url?u=https-3A__eur03.safelinks.protection.outlook.com_-3Furl-3Dhttps-253A-252F-252Fwww.genomicsengland.co.uk-252Fabout-2Dgenomics-2Dengland-252Fthe-2D100000-2Dgenomes-2Dproject-252F-26data-3D04-257C01-257Csegeg-2540mailman.kcl.ac.uk-257Cf9e6a91fac694ef1d12508da10bf3840-257C8370cf1416f34c16b83c724071654356-257C0-257C0-257C637840710716036121-257CUnknown-257CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0-253D-257C3000-26sdata-3DG7RlkcaDZgQ0jgtOCReNZWH8Sgbch9QU3EcaA0Dt-252FLE-253D-26reserved-3D0&d=DwMGaQ&c=D7ByGjS34AllFgecYw0iC6Zq7qlm8uclZFI0SqQnqBo&r=tf9MksA2A9wnBTXR1i5jSZxGLz7bbhC51Hd7GnvhmqQ&m=Zh0t62ojFUongfqJ4FhGAsrixvBTOfcuoLpeI-5pkrRBU8Sz5Y7sd2r2ctkcaYi8&s=jUAYPmmAHXZ0mI5if3ANKQmN1E_uglefdAaXbOX9_OY&e=" target="_blank" title="* this link opens in a new window/tab"><span style="color:#597FBA">100,000
 Genomes project</span> [eur03.safelinks.protection.outlook.com]</a><o:p></o:p></span></li><li class="MsoNormal" style="color:#232642;mso-margin-top-alt:auto;mso-margin-bottom-alt:auto;mso-list:l1 level1 lfo3;background:white;box-sizing: inherit;font-size:1rem;padding-left:0.35rem">
<span style="font-size:12.0pt;font-family:"Helvetica Neue LT W05 55 Roman"">The genetics of cognitive and behavioral traits, using sequence and genotype data from UK Biobank and from large UK birth cohorts, the <a href="https://urldefense.proofpoint.com/v2/url?u=https-3A__eur03.safelinks.protection.outlook.com_-3Furl-3Dhttp-253A-252F-252Fwww.bristol.ac.uk-252Falspac-252F-26data-3D04-257C01-257Csegeg-2540mailman.kcl.ac.uk-257Cf9e6a91fac694ef1d12508da10bf3840-257C8370cf1416f34c16b83c724071654356-257C0-257C0-257C637840710716036121-257CUnknown-257CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0-253D-257C3000-26sdata-3DKR8ezo6WB8PGx3SxTLS1dwhGgPT-252BcSN2zBk3lMC3WQM-253D-26reserved-3D0&d=DwMGaQ&c=D7ByGjS34AllFgecYw0iC6Zq7qlm8uclZFI0SqQnqBo&r=tf9MksA2A9wnBTXR1i5jSZxGLz7bbhC51Hd7GnvhmqQ&m=Zh0t62ojFUongfqJ4FhGAsrixvBTOfcuoLpeI-5pkrRBU8Sz5Y7sd2r2ctkcaYi8&s=UpUTp06M4lU86lB7FBxrstSG-rs9_kgZy7SYLS9iFKM&e=" target="_blank" title="* this link opens in a new window/tab"><span style="color:#597FBA">Avon
 Longitudinal Study of Parents and Children</span> [eur03.safelinks.protection.outlook.com]</a> , the Millenium Cohort Study, and <a href="https://urldefense.proofpoint.com/v2/url?u=https-3A__eur03.safelinks.protection.outlook.com_-3Furl-3Dhttps-253A-252F-252Fborninbradford.nhs.uk-252F-26data-3D04-257C01-257Csegeg-2540mailman.kcl.ac.uk-257Cf9e6a91fac694ef1d12508da10bf3840-257C8370cf1416f34c16b83c724071654356-257C0-257C0-257C637840710716036121-257CUnknown-257CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0-253D-257C3000-26sdata-3DfUmBiGkmvMjJ4O4VJGEar4FmI18xH-252FA6j4Ru5xWtHqI-253D-26reserved-3D0&d=DwMGaQ&c=D7ByGjS34AllFgecYw0iC6Zq7qlm8uclZFI0SqQnqBo&r=tf9MksA2A9wnBTXR1i5jSZxGLz7bbhC51Hd7GnvhmqQ&m=Zh0t62ojFUongfqJ4FhGAsrixvBTOfcuoLpeI-5pkrRBU8Sz5Y7sd2r2ctkcaYi8&s=dg75UAjaDCokrSrdnIwvg0ZBJdYji4kzEDx4EVZoudA&e=" target="_blank" title="* this link opens in a new window/tab"><span style="color:#597FBA">Born
 in Bradford</span> [eur03.safelinks.protection.outlook.com]</a><o:p></o:p></span></li><li class="MsoNormal" style="color:#232642;mso-margin-top-alt:auto;mso-margin-bottom-alt:auto;mso-list:l1 level1 lfo3;background:white;box-sizing: inherit;font-size:1rem;padding-left:0.35rem">
<span style="font-size:12.0pt;font-family:"Helvetica Neue LT W05 55 Roman"">Population genetics and the genetic basis of complex diseases and traits in British South Asian populations, using data from the <a href="https://urldefense.proofpoint.com/v2/url?u=https-3A__eur03.safelinks.protection.outlook.com_-3Furl-3Dhttps-253A-252F-252Fwww.genesandhealth.org-252F-26data-3D04-257C01-257Csegeg-2540mailman.kcl.ac.uk-257Cf9e6a91fac694ef1d12508da10bf3840-257C8370cf1416f34c16b83c724071654356-257C0-257C0-257C637840710716036121-257CUnknown-257CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0-253D-257C3000-26sdata-3DJ1tn1mxl9mUaGYmU7mUxMlTfhOqUZs9SGnlMDAyqdE8-253D-26reserved-3D0&d=DwMGaQ&c=D7ByGjS34AllFgecYw0iC6Zq7qlm8uclZFI0SqQnqBo&r=tf9MksA2A9wnBTXR1i5jSZxGLz7bbhC51Hd7GnvhmqQ&m=Zh0t62ojFUongfqJ4FhGAsrixvBTOfcuoLpeI-5pkrRBU8Sz5Y7sd2r2ctkcaYi8&s=H2c1G5Yn5eMs9pnC5GwtGfzf1oVLow6dOI87cvGnD9M&e=" target="_blank" title="* this link opens in a new window/tab"><span style="color:#597FBA">Genes
 & Health project</span> [eur03.safelinks.protection.outlook.com]</a><o:p></o:p></span></li></ul>
<p style="background:white;box-sizing: inherit;margin-top:1rem;margin-bottom:1rem;font-variant-ligatures: normal;font-variant-caps: normal;orphans: 2;text-align:start;widows: 2;-webkit-text-stroke-width: 0px;text-decoration-thickness: initial;text-decoration-style: initial;text-decoration-color: initial;word-spacing:0px">
<span style="font-size:12.0pt;font-family:"Helvetica Neue LT W05 55 Roman";color:#232642"> This postdoc position is funded through a grant from the Simons Foundation Autism Research Initiative, as part of a large collaborative project investigating the causes
 of sex differences in autism. The postdoctoral fellow will collaborate closely with colleagues at the Autism Research Centre in Cambridge (Simon Baron-Cohen and Varun Warrier), the Hurles group at the Sanger, and the Autism Sequencing Consortium. The project
 will entail analysing large-scale exome/genome-sequencing data and genotype data from autism and developmental disorder cohorts (including a new UK-based study, Spectrum10K) and from population-based studies such as ALSPAC and UK Biobank. <o:p></o:p></span></p>
<p class="MsoNormal"><b><span style="font-size:12.0pt;font-family:"Helvetica Neue LT W05 55 Roman";color:#232642;mso-fareast-language:EN-GB">Salary per annum:
</span></b><span style="font-size:12.0pt;font-family:"Helvetica Neue LT W05 55 Roman";color:#232642;mso-fareast-language:EN-GB">£33,272 - £41,709<o:p></o:p></span></p>
<p class="MsoNormal"><b><span style="font-size:12.0pt;font-family:"Helvetica Neue LT W05 55 Roman";color:#232642;mso-fareast-language:EN-GB">Contract Length:
</span></b><span style="font-size:12.0pt;font-family:"Helvetica Neue LT W05 55 Roman";color:#232642;mso-fareast-language:EN-GB">2.5 years with possibility of extension<o:p></o:p></span></p>
<p class="MsoNormal"><b><span style="font-size:12.0pt;font-family:"Helvetica Neue LT W05 55 Roman";color:#232642;mso-fareast-language:EN-GB">Closing Date:
</span></b><span style="font-size:12.0pt;font-family:"Helvetica Neue LT W05 55 Roman";color:#232642;mso-fareast-language:EN-GB">21 April 2022</span><span style="font-size:13.0pt;font-family:"Helvetica Neue LT W05 55 Roman";color:#232642;mso-fareast-language:EN-GB"><o:p></o:p></span></p>
<p class="MsoNormal"><o:p> </o:p></p>
<p class="MsoNormal"><span style="mso-fareast-language:EN-GB">-- The Wellcome Sanger Institute is operated by Genome Research Limited, a charity registered in England with number 1021457 and a company registered in England with number 2742969, whose registered
 office is 215 Euston Road, London, NW1 2BE. <o:p></o:p></span></p>
</div>



-- 
 The Wellcome Sanger Institute is operated by Genome Research 
 Limited, a charity registered in England with number 1021457 and a 
 company registered in England with number 2742969, whose registered 
 office is 215 Euston Road, London, NW1 2BE. 

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