Associated Papers
Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes.
Lewis MA et al.
Bmc Medical Genomics, 2018
30180840 (PubMed )
Supplement: 12920_2018_395_MOESM15_ESM.xls › Table_S11
Somatic Variations in Cervical Cancers in Indian Patients.
Das P et al.
Plos One, 2016
27829003 (PubMed )
Supplement: pone.0165878.s001.xlsx › somatic_cosmic_hit.list
Lysoplex: An efficient toolkit to detect DNA sequence variations in the autophagy-lysosomal pathway.
Di Fruscio G et al.
Autophagy, 2015
26075876 (PubMed )
Supplement: kaup-11-06-1043077-s001.zip › 1043077_supplemental_files › TABLE_S6.xlsx › results
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