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Biology subjects

Babinski, M.

Publications and source records attributed to Babinski, M..

3 recordsLinked to original sources

Learning the language of proteins and predicting the impact of mutations

Mutations in proteins directly impact their structure and function. Understanding the "language" of proteins, or the sequence to function (genotype-phenotype) relationship has many real-world applications. One set of applications includes those in biodefense, such as biological threat detection and biosurveillance, antibody engineering, and medical countermeasure development. In this study, we present a novel language model-based approach that can rapidly analyze vast collections of sequences, and make near real-time functional predictions that compare favorably to those made using conventional bioinformatic and experimental methods. Our findings reveal that tailored protein language models can predict protein mutation phenotypes, such as binding affinity or level of expression, when they are trained with high-throughput functional data. Protein language models applied to viral genomes can also discern the lineage within a family (e.g., sarbecovirus sequences). Coupled with sequenced-based biosurveillance, this type of model may provide early warning signals of potential zoonotic spillovers (i.e. host jumping) or "escape" from existing medical countermeasures posed by novel mutations. This research not only underscores the potential of ML and language models in addressing pressing challenges in understanding the mapping of sequence to function, but further elucidates their potential application in accelerating the response to biological threats as they evolve.

bioinformatics↗

Blueberry and cranberry pangenomes as a resource for future genetic studies and breeding efforts

Domestication of cranberry and blueberry began in the United States in the early 1800s and 1900s, respectively, and in part owing to their flavors and health-promoting benefits are now cultivated and consumed worldwide. The industry continues to face a wide variety of production challenges (e.g. disease pressures) as well as a demand for higher-yielding cultivars with improved fruit quality characteristics. Unfortunately, molecular tools to help guide breeding efforts for these species have been relatively limited compared with those for other high-value crops. Here, we describe the construction and analysis of the first pangenome for both blueberry and cranberry. Our analysis of these pangenomes revealed both crops exhibit great genetic diversity, including the presence-absence variation of 48.4% genes in highbush blueberry and 47.0% genes in cranberry. Auxiliary genes, those not shared by all cultivars, are significantly enriched with molecular functions associated with disease resistance and the biosynthesis of specialized metabolites, including compounds previously associated with improving fruit quality traits. The discovery of thousands of genes, not present in the previous reference genomes for blueberry and cranberry, will serve as the basis of future research and as potential targets for future breeding efforts. The pangenome, as a multiple-sequence alignment, as well as individual annotated genomes, are publicly available for analysis on the Genome Database for Vaccinium - a curated and integrated web-based relational database. Lastly, the core-gene predictions from the pangenomes will serve useful to develop a community genotyping platform to guide future molecular breeding efforts across the family.

genomics↗

You can move, but you can't hide: identification of mobile genetic elements with geNomad

Identifying and characterizing mobile genetic elements (MGEs) in sequencing data is essential for understanding their diversity, ecology, biotechnological applications, and impact on public health. Here, we introduce geNomad, a classification and annotation framework that combines information from gene content and a deep neural network to identify sequences of plasmids and viruses. geNomad uses a large dataset of marker proteins to provide functional gene annotation and taxonomic assignment of viral genomes. Using a conditional random field model, geNomad also detects proviruses integrated into host genomes with high precision. In benchmarks that included diverse MGE and chromosome sequences, geNomad significantly outperformed other tools in all evaluated clades of plasmids and viruses. Leveraging geNomads speed and scalability, we were able to process public metagenomes and metatranscriptomes, leading to the discovery of millions of new viruses and plasmids that are available through the IMG/VR and IMG/PR databases. We anticipate that geNomad will enable further advancements in MGE research, and it is available at https://portal.nersc.gov/genomad.

bioinformatics↗