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2. Predicting venous thromboembolism risk from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges

4. Assessing the performance of in silico methods for predicting the pathogenicity of variants in the gene CHEK2, among Hispanic females with breast cancer

5. Assessment of predicted enzymatic activity of α‐ N ‐acetylglucosaminidase variants of unknown significance for CAGI 2016

6. Assessment of patient clinical descriptions and pathogenic variants from gene panel sequences in the CAGI‐5 intellectual disability challenge

7. CAGI SickKids challenges: Assessment of phenotype and variant predictions derived from clinical and genomic data of children with undiagnosed diseases

9. Assessment of methods for predicting the effects of PTEN and TPMT protein variants

10. Assessing computational predictions of the phenotypic effect of cystathionine‐beta‐synthase variants

11. Working toward precision medicine: Predicting phenotypes from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges

16. Matching phenotypes to whole genomes: Lessons learned from four iterations of the personal genome project community challenges

17. Lessons from the CAGI‐4 Hopkins clinical panel challenge

18. Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI

19. Predicting venous thromboembolism risk from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges

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