Apurba Shil, PhD
@ApurbaShil19
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Post Doc @ Aarhus University 👨💻🤸
Arhus, Denmark
Joined June 2021
Online workshop on GWAS, heritability analysis and prediction on Tuesday 1st and Wednesday 2nd April. Each day runs from 8.30-11AM BST. Attendance is free; find out more details and register at EventBrite ( https://t.co/iPHJ3ZA3Ox)
eventbrite.com
Doug Speed and David Balding will present an online version of their workshop on GWAS, heritability analysis and prediction.
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Still time to apply for the SMARTbiomed postdoc/assistant prof jobs based in Aarhus, Copenhagen and Oxford - causal inference, risk prediction, machine learning in applications for any common complex disease. At Oxford work with any group leader @bdi_oxford, @OxfordStats .
New Pioneer Centre, SMARTbiomed, will be advancing applications in medicine and is a research collaboration between @UniofOxford, @koebenhavns_uni and @AarhusUni, anchored at Aarhus BSS. You can join the research team. See more at https://t.co/W8rCZpHjh5.
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🚀 Join my team at Karolinska Institutet as a Postdoctoral Researcher in genomics! Work on neurodevelopmental disorders in an innovative, collaborative environment. We tailor training to your goals and welcome diverse backgrounds. Apply now: https://t.co/XPoTfBPWeC
ki.varbi.com
Do you want to contribute to improving human health? The position is available in the research group led by Senior Researcher Kristiina Tammimies at the Department of Women’s and Children’s Health
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Trying to use some function of disgenet2r, but unable to access it through the API (for the past few days+API key 🔐 can't be generated). Any update? @DisGeNET
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A simple and integrative ranking approach (with >72% accuracy) to prioritize clinically relevant ASD candidate variants.. It can be used in WES/WGS pipelines [Sorry about Fig. 3B and Fig. 4]...The performance was assessed in the WES data from https://t.co/nl8oJXK0kT.
AutScore- An integrative scoring approach for prioritization of ultra-rare autism spectrum disorder candidate variants from whole exome sequencing data https://t.co/xaZGwBACwV
#medRxiv
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Comparison of three bioinformatics tools in the detection of ASD candidate variants from whole exome sequencing data
pubmed.ncbi.nlm.nih.gov
Autism spectrum disorder (ASD) is a heterogenous multifactorial neurodevelopmental condition with a significant genetic susceptibility component. Thus, identifying genetic variations associated with...
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@bengurionu @fohsbgu We used WES data from ASD-affected Israeli families registered at
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Happy to share the first paper (from my Ph.D. thesis) entitled "Comparison of three bioinformatics tools in the detection of ASD candidate variants from whole exome sequencing data." From @bengurionu @fohsbgu ; Idan's Lab: https://t.co/6KwHpbwB8e
https://t.co/x0ITNi1v8H
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Genetic Elucidation of Ultrasonography Fetal Anomalies in Children with Autism Spectrum Disorder https://t.co/WQ1v2QD8XQ
#medRxiv
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Genetic Elucidation of Ultrasonography Fetal Anomalies in Children with Autism Spectrum Disorder
medrxiv.org
Recent evidence suggests that certain fetal anomalies detected upon prenatal ultrasound screenings may be associated with autism spectrum disorder (ASD). In this cross-sectional study, we aimed to...
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What a great first day of #INSAR2023 ! We had great attendance at the #insar_culturaldiversity preconference workshop! Hope to meet more attendees in the days to come!
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Thankful for this gathering, collaboration, & space to discuss culture, language & autism @AutismINSAR #INSAR_CulturalDiversity committee C-CAP mentoring program and for amazing mentors @gulnoza_ry & Li Yi & colleagues Sofia & Apurba 🙏🏼🙌🏼
Gulnoza Yakubova, Li Yi, Veronica Kang, Sofia Baena Medina, and Apuraba Shil presenting on the INSAR C-CAP mentoring program @gulnoza_ry @VeronicaYKang #insar_culturaldiversity #INSAR2023
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Gulnoza Yakubova, Li Yi, Veronica Kang, Sofia Baena Medina, and Apuraba Shil presenting on the INSAR C-CAP mentoring program @gulnoza_ry @VeronicaYKang #insar_culturaldiversity #INSAR2023
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@fohsbgu @bengurionu Here we compared the concordance and effectiveness of the 3 tools (1. ACMG/AMP SNV interpretation tools InterVar and TAPES and 2. In-house tool Psi-Variant) to detect ASD candidate SNVs from WES data.
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Effectiveness of three bioinformatics tools in the detection of ASD candidate variants from whole exome sequencing data https://t.co/ZjdTOVoSWI
#medRxiv
medrxiv.org
Background Autism spectrum disorder (ASD) is a heterogenous multifactorial neurodevelopmental condition with a significant genetic susceptibility component. Thus, identifying genetic variations...
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Excited to share the preprint version of a recent manuscript (from the Ph.D. thesis) we submitted to a journal a few days back. @fohsbgu @bengurionu
medrxiv.org
Background Autism spectrum disorder (ASD) is a heterogenous multifactorial neurodevelopmental condition with a significant genetic susceptibility component. Thus, identifying genetic variations...
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