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Zinger, T.

Publications and source records attributed to Zinger, T..

5 recordsLinked to original sources

DNT: Diploid Genomic Foundation Model

Clinical interpretation of genetic variation depends on the diploid genotype, including zygosity, allele dosage and whether multiple variants occur in cis on the same homologue or in trans on different homologues. Most genomic language models process haploid sequences or combine independently encoded haplotypes downstream, so they do not directly represent the paired genotype in a single sequence. We introduce a reference-aligned diploid encoding for single-nucleotide variants (SNVs) and short insertions and deletions (indels), together with unphased and phase-retaining tokenizers that accept phased genotypes and convert them to single-sequence diploid representation. Using Nucleotide Transformer v3 backbones, we continue training 8-million- and 100-million-parameter models and evaluate an auxiliary Contrastive Phase Loss (CPL) designed to retain the phasing information of the variants in contextual representations. We evaluate on a novel compound-heterozygous benchmark containing 9,460 examples. Models whose inputs did not distinguish relative phase remained near chance, whereas our diploidic models improved discrimination with AUROC 0.649, compared to 0.506 for the vocabulary-adapted control. These findings establish a method for making diploid genotype information accessible to genomic language models, rather than a universal improvement in variant prediction; validation in naturally observed, accurately phased clinical cohorts remains necessary.

bioinformatics↗

GFMBench-API: A Standardized Interface for Benchmarking Genomic Foundation Models

The rapid scaling of Genomic Foundation Models (GFMs) has created a critical need for standardized evaluation frameworks. Current benchmarking practices are often fragmented, relying on model-specific preprocessing and inconsistent metric implementations that hinder reproducible comparisons. We present GFMBench-API, a high-level Python interface designed to unify the evaluation lifecycle of GFMs. GFMBench-API provides a modular "middleware" architecture that decouples model-specific tokenization and embedding logic from task-specific data streams and performance metrics. By standardizing the input/output schemas for common genomic tasks, such as regulatory element prediction, variant effect scoring, and long-range interaction mapping, GFMBench-API enables researchers to integrate new models or tasks with minimal "glue code." Our interface ensures mathematical consistency across evaluations, providing a robust foundation for the transparent and systematic benchmarking of GFMs.

genomics↗

i6A-seq maps N6-isopentenyladenosine and uncovers its role as a regulator of mRNA stability through recruitment of DIS3L2

Dynamic post-transcriptional RNA modifications are crucial regulators of RNA metabolism and cell fate. Recent advances in sequencing, combined with antibody, enzymatic, or chemical approaches, have enabled transcriptome-wide mapping of these modifications. While prevalent in tRNAs and rRNAs, a growing number of modifications also adorn lower-abundance mRNA transcripts. Global mapping efforts, particularly for N6-methyladenosine (m6A), uncovered the affected mechanisms governing RNA metabolism, shedding light on novel, modification-dependent, modes of gene regulation. N6-isopentenyladenosine (i6A) is a conserved tRNA modification involved in translation fidelity and efficiency. i6A depletion is linked to mitochondrial defects and human diseases. Current i6A detection methods are low-throughput, and its lack of base-pairing effects makes sequencing-based identification challenging. Here we developed a novel and robust mapping technique, i6A-seq, a method that utilizes antibody-mediated enrichment and iodine chemical labeling to generate a reverse transcription signature, enabling transcriptome-wide i6A detection. Our global mapping revealed hundreds of i6A sites in human and mouse mRNA, indicating its presence in this RNA species, with conserved isopentenylome features. These sites exhibit a typical consensus sequence, primarily in coding transcripts (CDS), preferentially within lysine codons. Consistent with its role in tRNA, tRNA-isopentenyltransferase (TRIT1) also appears to install i6A in mRNA. Manipulation of TRIT1 revealed that i6A regulates the expression of a subset of genes through mRNA decay, specifically those isopentenylated at the CDS and translated on ER-bound ribosomes. Importantly, DIS3 like 3-5 exoribonuclease 2 (DIS3L2), an RNA exoribonuclease known to regulate ER-translated mRNA, was identified as the first i6A reader protein. Our findings introduce i6A as a new modified nucleotide that decorates mRNA, allowing us to decipher its regulatory roles in gene expression. This study not only establishes the presence and location of i6A in mRNA, but also uncovers its first functional mechanism. Similar to the knowledge accumulated on m6A, this work paves the way for further discoveries with potential relevance for understanding gene regulation, disease diagnosis, and therapy.

molecular biology↗

Performance of the rapid Nucleic Acid Amplification by Abbott ID NOW COVID-19 in nasopharyngeal swabs transported in viral media and dry nasal swabs, in a New York City academic institution

The recent emergence of the SARS-CoV-2 pandemic has posed formidable challenges for clinical laboratories seeking reliable laboratory diagnostic confirmation. The swift advance of the crisis in the United States has led to Emergency Use Authorization (EUA) facilitating the availability of molecular diagnostic assays without the more rigorous examination to which tests are normally subjected prior to FDA approval. Our laboratory currently uses two real time RT-PCR platforms, the Roche Cobas SARS-CoV2 and the Cepheid Xpert Xpress SARS-CoV-2. Both platforms demonstrate comparable performance; however, the run times for each assay are 3.5 hours and 45 minutes, respectively. In search for a platform with shorter turnaround time, we sought to evaluate the recently released Abbott ID NOW COVID-19 assay which is capable of producing positive results in as little as 5 minutes. We present here the results of comparisons between Abbott ID NOW COVID-19 and Cepheid Xpert Xpress SARS-CoV-2 using nasopharyngeal swabs transported in viral transport media and comparisons between Abbott ID NOW COVID-19 and Cepheid Xpert Xpress SARS-CoV-2 using nasopharyngeal swabs transported in viral transport media for Cepheid and dry nasal swabs for Abbott ID NOW. Regardless of method of collection and sample type, Abbott ID NOW COVID-19 had negative results in a third of the samples that tested positive by Cepheid Xpert Xpress when using nasopharyngeal swabs in viral transport media and 45% when using dry nasal swabs.

microbiology↗

Inferring Population Genetics Parameters of Evolving Viruses Using Time-series Data

1With the advent of deep sequencing techniques, it is now possible to track the evolution of viruses with ever-increasing detail. Here we present FITS (Flexible Inference from Time-Series) - a computational framework that allows inference of either the fitness of a mutation, the mutation rate or the population size from genomic time-series sequencing data. FITS was designed first and foremost for analysis of either short-term Evolve & Resequence (E&R) experiments, or for rapidly recombining populations of viruses. We thoroughly explore the performance of FITS on noisy simulated data, and highlight its ability to infer meaningful information even in those circumstances. In particular FITS is able to categorize a mutation as Advantageous, Neutral or Deleterious. We next apply FITS to empirical data from an E&R experiment on poliovirus where parameters were determined experimentally and demonstrate extremely high accuracy in inference. We highlight the ease of use of FITS for step-wise or iterative inference of mutation rates, population size, and fitness values for each mutation sequenced, when deep sequencing data is available at multiple time-points.\n\nAvailabilityFITS is written in C++ and is available both with a highly user friendly graphical user interface but also as a command line program that allows parallel high throughput analyses. Source code, binaries (Windows and Mac) and complementary scripts, are available from GitHub at https://github.com/SternLabTAU/FITS.\n\nContactsternadi@tau.ac.il

evolutionary biology↗