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  1. The Complete Genomic Sequence of Microbial Transglutaminase Producer, Streptomyces mobaraensis DSM40587

    Actinomycetes are remarkable natural sources of active natural molecules and enzymes of considerable industrial value. Streptomyces mobaraensis is...

    **-long Feng, Rui-qi Zhang, ... Jianzhao Qi in Biochemical Genetics
    Article 02 August 2023
  2. Genomic sequence capture of Plasmodium relictum in experimentally infected birds

    Background

    Sequencing parasite genomes in the presence of host DNA is challenging. Sequence capture can overcome this problem by using RNA probes that...

    Vincenzo A. Ellis, Victor Kalbskopf, ... Vaidas Palinauskas in Parasites & Vectors
    Article Open access 29 July 2022
  3. Genomic Ancestry as Biomarkers

    The influence of ethnicity on diabetic retinopathy has been studied for decades with controversial results. Different populations report different...
    Deborah Conte Santos in Biomarkers in Diabetes
    Reference work entry 2023
  4. Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy

    We performed whole-genome sequencing (WGS) in 327 children with cerebral palsy (CP) and their biological parents. We classified 37 of 327 (11.3%)...

    Darcy L. Fehlings, Mehdi Zarrei, ... Stephen W. Scherer in Nature Genetics
    Article 29 March 2024
  5. Screening Host Genomic Data for Wolbachia Infections

    Less than a decade ago, the production of Wolbachia genomic assemblies was tedious, time-consuming, and expensive. The production of Wolbachia...
    Federica Valerio, Victoria G. Twort, Anne Duplouy in Wolbachia
    Protocol 2024
  6. Genomic analysis of the international high-risk clonal lineage Klebsiella pneumoniae sequence type 395

    Background

    Klebsiella pneumoniae , which is frequently associated with hospital- and community-acquired infections, contains multidrug-resistant...

    Elvira R. Shaidullina, Michael Schwabe, ... Mikhail V. Edelstein in Genome Medicine
    Article Open access 13 February 2023
  7. Sequence Alignment

    Sequence alignment is an essential computational step before performing evolutionary analysis of genomic sequences and structural analysis of...
    Chapter 2022
  8. Construction of Genomic and Sub-Genomic Dengue Infectious Replicons

    Dengue replicons are powerful tools used in studying virus biology as well as in high-throughput screening of drug candidates. Replicon constructs...
    Thu M. Cao, Richard J. Kuhn in Dengue Virus
    Protocol 2022
  9. Sequence dependencies and mutation rates of localized mutational processes in cancer

    Background

    Cancer mutations accumulate through replication errors and DNA damage coupled with incomplete repair. Individual mutational processes often...

    Gustav Alexander Poulsgaard, Simon Grund Sørensen, ... Jakob Skou Pedersen in Genome Medicine
    Article Open access 17 August 2023
  10. The complete genome sequence of tomato necrotic ringspot virus in chilli in Thailand derived from next-generation sequencing

    Tomato necrotic ringspot virus (TNRV) was first reported in Thailand in 2011, where it continues to reduce the yield and quality of pepper and tomato...

    Phoowanarth Maneechoat, Pissawan Chiemsombat, ... Scott Adkins in Archives of Virology
    Article 07 March 2024
  11. Complete genome sequence of a novel robigovirus infecting Mentha arvensis

    The complete genomic sequence of a novel robigovirus, provisionally named “Mentha arvensis robigovirus 1” (MARV1), was determined by combining...

    Hai-Tao Weng, Yi-Yuan Li, ... Zhong-Tian Xu in Archives of Virology
    Article 05 January 2024
  12. Genomic Ancestry as Biomarkers

    The influence of ethnicity on diabetic retinopathy has been studied for decades with controversial results. Different populations report different...
    Deborah Conte Santos in Biomarkers in Diabetes
    Living reference work entry 2022
  13. Personal transcriptome variation is poorly explained by current genomic deep learning models

    Genomic deep learning models can predict genome-wide epigenetic features and gene expression levels directly from DNA sequence. While current models...

    Connie Huang, Richard W. Shuai, ... Nilah M. Ioannidis in Nature Genetics
    Article Open access 30 November 2023
  14. Oncogenic Genomic Changes in Cancer

    A common cause of all cancers leads us to a common definition. This definition is mutation. Cancer cells tend to constantly resist irregularity under...
    Abdulbaki Yildirim, Hilal Akalin, Munis Dundar in Oncology: Genomics, Precision Medicine and Therapeutic Targets
    Chapter 2023
  15. Benchmarking of deep neural networks for predicting personal gene expression from DNA sequence highlights shortcomings

    Deep learning methods have recently become the state of the art in a variety of regulatory genomic tasks 1 6 , including the prediction of gene...

    Alexander Sasse, Bernard Ng, ... Sara Mostafavi in Nature Genetics
    Article 30 November 2023
  16. Genomic Mosaicism of the Brain: Origin, Impact, and Utility

    Genomic mosaicism describes the phenomenon where some but not all cells within a tissue harbor unique genetic mutations. Traditionally, research...

    Jared H. Graham, Johannes C. M. Schlachetzki, ... Martin W. Breuss in Neuroscience Bulletin
    Article Open access 29 October 2023
  17. Genomic surveillance for antimicrobial resistance — a One Health perspective

    Antimicrobial resistance (AMR) — the ability of microorganisms to adapt and survive under diverse chemical selection pressures — is influenced by...

    Steven P. Djordjevic, Veronica M. Jarocki, ... Benjamin P. Howden in Nature Reviews Genetics
    Article 25 September 2023
  18. Genomic Instability in Carcinogenesis

    Genomic instability is one of the hallmarks of cancer. Several theories have been put forth to ascertain this departure from the normal state as...
    Reference work entry 2022
  19. Genomic newborn screening for rare diseases

    Rare diseases are a leading cause of infant mortality and lifelong disability. To improve outcomes, timely diagnosis and effective treatments are...

    Zornitza Stark, Richard H. Scott in Nature Reviews Genetics
    Article 29 June 2023
  20. The value of genomic testing in severe childhood speech disorders

    With increasing gene discoveries for severe speech disorders, genomic testing can alter the diagnostic and clinical paradigms, enabling better life...

    Yan Meng, Stephanie Best, ... Ilias Goranitis in European Journal of Human Genetics
    Article Open access 02 February 2024
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