User profiles for author:"Gunjan Baid"
 | Gunjan BaidInductive Bio Verified email at inductive.bio Cited by 1667 |
[PDF][PDF] Scaling autoregressive models for content-rich text-to-image generation
Abstract We present the Pathways [1] Autoregressive Text-to-Image (Parti) model, which
generates high-fidelity photorealistic images and supports content-rich synthesis involving …
generates high-fidelity photorealistic images and supports content-rich synthesis involving …
A draft human pangenome reference
Abstract Here the Human Pangenome Reference Consortium presents a first draft of the
human pangenome reference. The pangenome contains 47 phased, diploid assemblies …
human pangenome reference. The pangenome contains 47 phased, diploid assemblies …
Ultrarapid nanopore genome sequencing in a critical care setting
Genetic Diagnoses in Critical Care Because a genetic diagnosis can guide clinical
management and improve prognosis in critically ill patients, much effort has gone into …
management and improve prognosis in critically ill patients, much effort has gone into …
Haplotype-aware variant calling with PEPPER-Margin-DeepVariant enables high accuracy in nanopore long-reads
Long-read sequencing has the potential to transform variant detection by reaching currently
difficult-to-map regions and routinely linking together adjacent variations to enable read …
difficult-to-map regions and routinely linking together adjacent variations to enable read …
DeepConsensus improves the accuracy of sequences with a gap-aware sequence transformer
Circular consensus sequencing with Pacific Biosciences (PacBio) technology generates
long (10–25 kilobases), accurate 'HiFi'reads by combining serial observations of a DNA …
long (10–25 kilobases), accurate 'HiFi'reads by combining serial observations of a DNA …
Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencing
Whole-genome sequencing (WGS) can identify variants that cause genetic disease, but the
time required for sequencing and analysis has been a barrier to its use in acutely ill patients …
time required for sequencing and analysis has been a barrier to its use in acutely ill patients …
[PDF][PDF] PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regions
ND Olson, J Wagner, J McDaniel, SH Stephens… - Cell genomics, 2022 - cell.com
Summary The precisionFDA Truth Challenge V2 aimed to assess the state of the art of
variant calling in challenging genomic regions. Starting with FASTQs, 20 challenge …
variant calling in challenging genomic regions. Starting with FASTQs, 20 challenge …
Gaps and complex structurally variant loci in phased genome assemblies
D Porubsky, MR Vollger, WT Harvey… - Genome …, 2023 - genome.cshlp.org
There has been tremendous progress in phased genome assembly production by
combining long-read data with parental information or linked-read data. Nevertheless, a …
combining long-read data with parental information or linked-read data. Nevertheless, a …
Haplotype-aware variant calling enables high accuracy in nanopore long-reads using deep neural networks
Long-read sequencing has the potential to transform variant detection by reaching currently
difficult-to-map regions and routinely linking together adjacent variations to enable read …
difficult-to-map regions and routinely linking together adjacent variations to enable read …
DeepTrio: variant calling in families using deep learning
Every human inherits one copy of the genome from their mother and another from their
father. Parental inheritance helps us understand the transmission of traits and genetic …
father. Parental inheritance helps us understand the transmission of traits and genetic …