All Stories

  1. Whole genome sequencing identifies novel structural variant in a large Indian family affected with X-linked agammaglobulinemia
  2. High throughput detection and genetic epidemiology of SARS-CoV-2 using COVIDSeq next-generation sequencing
  3. DALIA- a comprehensive resource of Disease Alleles in Arab population
  4. Normative range of blood biochemical parameters in urban Indian school-going adolescents
  5. Utility of whole-exome sequencing in detecting novel compound heterozygous mutations in COL7A1 among families with severe recessive dystrophic epidermolysis bullosa in India - implications on diagnosis, prognosis and prenatal testing
  6. A new strain of white spot syndrome virus affecting Litopenaeus vannamei in Indian shrimp farms
  7. A founder mutation MLC1 c.736delA associated with megalencephalic leukoencephalopathy with subcortical cysts-1 in north Indian kindred
  8. Pharmacogenetic landscape of DPYD variants in south Asian populations by integration of genome-scale data
  9. Computational Modeling of Small Molecule Inhibitors of Mitochondrial Fusion
  10. Genetic epidemiology of familial Mediterranean fever through integrative analysis of whole genome and exome sequences from Middle East and North Africa
  11. From genomes to genomic medicine: enabling personalized and precision medicine in the Middle East
  12. Egyptian tale from India: application of whole-exome sequencing in diagnosis of atypical familial Mediterranean fever
  13. Case Report: Whole exome sequencing identifies a novel frameshift insertion c.1325dupT (p.F442fsX2) in the tyrosine kinase domain of BTK gene in a young Indian individual with X-linked agammaglobulinemia
  14. Landscape of warfarin and clopidogrel pharmacogenetic variants in Qatari population from whole exome datasets
  15. Case Report: Whole exome sequencing identifies variation c.2308G>A p.E770K in RAG1 associated with B- T- NK+ severe combined immunodeficiency
  16. Case Report: Application of whole exome sequencing for accurate diagnosis of rare syndromes of mineralocorticoid excess
  17. Case Report: Whole exome sequencing reveals a novel frameshift deletion mutation p.G2254fs in COL7A1 associated with autosomal recessive dystrophic epidermolysis bullosa
  18. Long noncoding RNAs could be potential key players in the pathophysiology of Sjögren's syndrome
  19. Does the buck stop with the bugs?: an overview of microbial dysbiosis in rheumatoid arthritis
  20. Case Report: Whole exome sequencing helps in accurate molecular diagnosis in siblings with a rare co-occurrence of paternally inherited 22q12 duplication and autosomal recessive non-syndromic ichthyosis.
  21. mit-o-matic: A Comprehensive Computational Pipeline for Clinical Evaluation of Mitochondrial Variations from Next-Generation Sequencing Datasets
  22. Personal genomes, participatory genomics and the anonymity-privacy conundrum
  23. Short Stories on Zebrafish Long Noncoding RNAs
  24. Joining the long shots: emerging evidence on the role of long noncoding RNAs in rheumatoid arthritis
  25. Comparative analysis of human mitochondrial methylomes shows distinct patterns of epigenetic regulation in mitochondria
  26. Data-mining of potential antitubercular activities from molecular ingredients of traditional Chinese medicines
  27. Personal genomes to precision medicine
  28. Comparative analysis of human mitochondrial methylome show distinct patterns of epigenetic regulation in mitochondria
  29. Cheminformatics Models for Inhibitors ofSchistosoma mansoniThioredoxin Glutathione Reductase
  30. Time for the zebrafish ENCODE
  31. Distinct Patterns of Genetic Variations in Potential Functional Elements in Long Noncoding RNAs
  32. Draft Genome Sequence of a Multidrug-Resistant Clinical Isolate of Mycobacterium tuberculosis Belonging to a Novel Spoligotype
  33. Cheminformatic models based on machine learning for pyruvate kinase inhibitors of Leishmania mexicana
  34. MitoLSDB: A Comprehensive Resource to Study Genotype to Phenotype Correlations in Human Mitochondrial DNA Variations
  35. Predictive modeling of anti-malarial molecules inhibiting apicoplast formation
  36. Systematic Transcriptome Wide Analysis of lncRNA-miRNA Interactions
  37. Long Non-Coding RNAs in Infection Biology
  38. Pharmacogenomics in the Era of Personal Genomics: A Quick Guide to Online Resources and Tools
  39. Non-invasive detection of mycobacterium tuberculosis using IR and NIR spectroscopy
  40. Computational analysis and predictive modeling of small molecule modulators of microRNA
  41. Integrative transcriptome analysis suggest processing of a subset of long non-coding RNAs to small RNAs
  42. Antagonism of microRNA Function in Zebrafish Embryos by Using Locked Nucleic Acid Enzymes (LNAzymes)
  43. Potential G-quadruplexes in the human long non-coding transcriptome
  44. The Sri Lankan Personal Genome Project: an overview
  45. miRvar: A comprehensive database for genomic variations in microRNAs
  46. “Locked onto the Target”: Increasing the Efficiency of Antagomirzymes Using Locked Nucleic Acid Modifications
  47. Modulation of microRNA function by synthetic ribozymes
  48. MicroRNAs: novel therapeutic targets in neurodegenerative diseases
  49. TBrowse: An integrative genomics map of Mycobacterium tuberculosis
  50. Prediction of viral microRNA precursors based on human microRNA precursor sequence and structural features
  51. SCA-LSVD: A repeat-oriented locus-specific variation database for genotype to phenotype correlations in spinocerebellar ataxias
  52. dbSMR: a novel resource of genome-wide SNPs affecting microRNA mediated regulation
  53. Antagomirzymes: Oligonucleotide Enzymes That Specifically Silence MicroRNA Function
  54. Antagomirzymes: Oligonucleotide Enzymes That Specifically Silence MicroRNA Function
  55. Host-virus genome interactions: macro roles for microRNAs
  56. microRNA: an Emerging Therapeutic
  57. microRNAs in viral oncogenesis