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From Algorithms to Discovery in Genome-Scale Biology and Medicine 2022

single-cell genomics researchers, computational biologists, cancer genomics researchers, translational clinico-genomics scientists, systems biologists, proteomics researchers, bioinformatics engineers

spatial omics clustering; spatial transcriptomics deconvolution; cis-regulatory element conservation; chemical bioactivity embeddings; integrated iCell network analysis; single-cell 3D epigenomics imputation; reference-free k-mer variant detection; in silico clinical trial platforms; phospho-QTL genetic mapping; tyrosine kinase interactome mapping; ancient DNA phenotype inference; variant deleteriousness prediction

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BANKSY: A Spatial Omics Algorithm that Unifies Cell Type Clustering and Tissue Domain SegmentationShyam Prabhakar47m
Algorithm constructs a product space of cell and neighborhood transcriptomes by appending k‑nearest‑neighbor averaged expression to each cell, then runs…
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Spatial Transcriptomics Identifies Neighbourhoods and Molecular Markers of Alveolar Damage...Martin Hemberg30m
Built a 600,000‑cell single‑cell lung atlas from 15 studies and applies NanoString GeoMx (≈18,000 probes) to 233 ROIs from 33 post‑mortem lungs scored as PRES…
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Landscapes of Human cis-regulatory Elements and Transcription Factor Binding Sites...Zhiping Weng39m
Built a registry of nearly 1 million candidate cis‑regulatory elements from ENCODE data, then aligns them with a 240‑mammal CACTUS alignment and mammal PhyloP…
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Formatting Biological Big Data to Enable (Personalized) Systems PharmacologyPatrick Aloy36m
A publicly released resource called Chemical Checker turns experimental bioactivity for ~1,000,000 small molecules into 25 complementary 128‑dimensional vector…
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Understanding Molecular Complexity for Precision MedicineNatasa Przulj33m
Graph topology methods convert heterogeneous omics into an iCell integrated network using graph-regularized NMTF and graphlet counts; the top 500 most rewired…
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Machine Learning for Single-Cell 3D EpigenomicsJian Ma35m
Presents a concrete pipeline: a hypergraph model where hyperedge = cell+bin+bin encodes each single-cell Hi‑C contact, a graph/neural embedding (Higashi) that…
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A Statistical, Reference-Free Algorithm Subsumes Myriad Problems in Genome ScienceJulia Salzman27m
A unifying probabilistic model and a reference-free algorithm called gnomAD operates on raw FASTQ k-mers, builds contingency tables of upstream/downstream…
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Using Large-Scale Clinico-Genomics Data for in silico Clinical Trials and Precision OncologyJames Zou35m
A computational platform called Trial Pathfinder uses Flatiron EHR plus Foundation Medicine tumor panels to run millions of in silico trials, matching cohorts…
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Long-Range Propagation of Genetic Effects in Molecular NetworksAndreas Beyer33m
Cross of BY and RM yeast strains, matched RNA, protein (SWATH/DIA) and the first phospho-QTL layer, uses regression to remove abundance effects and random…
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A Binary Quantitative Interaction Mapping Approach: Elucidating Multiprotein Complexes in...Erich Wanker37m
Automated yeast two‑hybrid screens test ~70,000 pairings per week from a 17,000 human cDNA array but detect only ~20–25% of known interactions; a new LUCY…
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A Tyrosine Kinase Protein Interaction Map Reveals Targetable EGFR Network Oncogenesis in Lung CancerSourav Bandyopadhyay33m
A systematic AP‑MS survey of 90 tyrosine kinases in HEK293 cells (about 400+ AP‑MS experiments) yields a scored interaction map (CompPASS cutoff ~2.5) that…
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Computational Approaches to Study Interactions Between Mutagenic Processes and Cellular ProcessesTeresa Przytycka39m
Cancer mutational patterns are treated as quantitative traits and linked to expression, cell composition, and mutated subnetworks using concrete tools: 96…
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Mapping Biological Pathways Using Systematic Genetics and Cell BiologyBrenda Andrews34m
Systematic double-mutant mapping uses synthetic genetic array (SGA) and a colony size fitness proxy to quantify genetic interactions in yeast and yields ~1…
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Algorithms for Inferring Phenotypes from Ancient DNATony Capra43m
A deep learning pipeline predicts 3D Hi-C contact maps from 1 Mb of DNA and applies Akita deep learning model to Neanderthal, Denisovan and diverse modern…
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Predicting the Deleteriousness of Genomic Variants – Big and SmallMartin Kircher27m
CADD scores short variants by contrasting fixed human‑derived alleles with simulated de novo changes and integrates many annotations on a single continuous…
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Determining the Molecular Intermediates Between Genotype and PhenotypeDavid Knowles25m
Uses pooled RIP-seq on nine iPSC lines plus genotype estimates and a Bayesian beta‑binomial model (implemented in Pyro) to call allele‑specific RBP binding…
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How Genome 3D Organization Regulates Alternative Splicing?Gil Ast36m
Study demonstrates that genome 3D position links GC architecture to splicing mode: low-GC differential versus level GC architectures map to the nuclear…
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Distinct Gene Programs Underpinning ‘Disease Tolerance’ and ‘Resistance’ Against InfectionsIrit Gat-Viks25m
Identifies two co-activated lung gene programs — T program (disease tolerance) and R program (pathogen resistance) — from ~250 samples across 33 CC mouse…
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Exponentiating Single-Cell SequencingJimmie Ye35m
Generates a comprehensive single-cell lung atlas and pairs it with transcriptome-wide spatial profiling using Nanostring WTA of post-mortem COVID-19 lungs to…
Talk
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