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Author Details
Full Name
Miten Jain
Affiliation
Northeastern University
ORCID
Career Start Year
2011
Papers
47
H Index
23
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37066160
Multicellular, IVT-derived, unmodified human transcriptome for nanopore-direct RNA analysis.
bioRxiv
2024
36938359
Microbial isolation and characterization from two flex lines from the urine processor assembly onboard the international space station.
Biofilm
2023
37710018
Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation.
Nat Methods
2023
37745389
Local read haplotagging enables accurate long-read small variant calling.
bioRxiv
2023
37652985
Profiling of repetitive RNA sequences in the blood plasma of patients with cancer.
Nat Biomed Eng
2023
37612512
The complete sequence of a human Y chromosome.
Nature
2023
37205357
A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in <i>AFF3</i> as a significant cause of intellectual disability.
medRxiv
2023
36865218
Phased nanopore assembly with Shasta and modular graph phasing with GFAse.
bioRxiv
2023
34728536
Identification of high-confidence human poly(A) RNA isoform scaffolds using nanopore sequencing.
RNA
2022
35347328
Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencing.
Nat Biotechnol
2022
35720974
PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regions.
Cell Genom
2022
36203024
Advances in nanopore direct RNA sequencing.
Nat Methods
2022
35133172
Ultra-Rapid Nanopore Whole Genome Genetic Diagnosis of Dilated Cardiomyopathy in an Adolescent With Cardiogenic Shock.
Circ Genom Precis Med
2022
35244721
Nanopore ReCappable sequencing maps SARS-CoV-2 5' capping sites and provides new insights into the structure of sgRNAs.
Nucleic Acids Res
2022
35020984
Ultrarapid Nanopore Genome Sequencing in a Critical Care Setting.
N Engl J Med
2022
33467183
Real-Time Culture-Independent Microbial Profiling Onboard the International Space Station Using Nanopore Sequencing.
Genes (Basel)
2021
33794196
Pervasive cis effects of variation in copy number of large tandem repeats on local DNA methylation and gene expression.
Am J Hum Genet
2021
33851162
A new SARS-CoV-2 lineage that shares mutations with known Variants of Concern is rejected by automated sequence repository quality control.
bioRxiv
2021
33758101
miRNA-independent function of long noncoding pri-miRNA loci.
Proc Natl Acad Sci U S A
2021
34618430
Direct Nanopore Sequencing of Individual Full Length tRNA Strands.
ACS Nano
2021
34725481
Haplotype-aware variant calling with PEPPER-Margin-DeepVariant enables high accuracy in nanopore long-reads.
Nat Methods
2021
34446532
Synthesis of modified nucleotide polymers by the poly(U) polymerase Cid1: application to direct RNA sequencing on nanopores.
RNA
2021
34146471
A community challenge to evaluate RNA-seq, fusion detection, and isoform quantification methods for cancer discovery.
Cell Syst
2021
34085238
Adaptation of Human Ribosomal RNA for Nanopore Sequencing of Canonical and Modified Nucleotides.
Methods Mol Biol
2021
34047695
Inflammation drives alternative first exon usage to regulate immune genes including a novel iron-regulated isoform of <i>Aim2</i>.
Elife
2021
32520351
Metagenomic analysis of planktonic riverine microbial consortia using nanopore sequencing reveals insight into river microbe taxonomy and function.
Gigascience
2020
31936690
Off Earth Identification of Bacterial Populations Using 16S rDNA Nanopore Sequencing.
Genes (Basel)
2020
31819268
Author Correction: Nanopore native RNA sequencing of a human poly(A) transcriptome.
Nat Methods
2020
32775697
Permutational analysis of <i>Saccharomyces cerevisiae</i> regulatory elements.
Synth Biol (Oxf)
2020
32578857
Corrigendum to: Metagenomic analysis of planktonic riverine microbial consortia using nanopore sequencing reveals insight into river microbe taxonomy and function.
Gigascience
2020
32686750
Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes.
Nat Biotechnol
2020
32937144
A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions.
Am J Hum Genet
2020
32597959
Gaussian mixture model-based unsupervised nucleotide modification number detection using nanopore-sequencing readouts.
Bioinformatics
2020
31095620
Reading canonical and modified nucleobases in 16S ribosomal RNA using nanopore native RNA sequencing.
PLoS One
2019
29273626
MinION-based long-read sequencing and assembly extends the <i>Caenorhabditis elegans</i> reference genome.
Genome Res
2018
30461375
Resolving the complex Bordetella pertussis genome using barcoded nanopore sequencing.
Microb Genom
2018
29553574
Linear assembly of a human centromere on the Y chromosome.
Nat Biotechnol
2018
29431738
Nanopore sequencing and assembly of a human genome with ultra-long reads.
Nat Biotechnol
2018
28794860
MinION Analysis and Reference Consortium: Phase 2 data release and analysis of R9.0 chemistry.
F1000Res
2017
28218897
Mapping DNA methylation with high-throughput nanopore sequencing.
Nat Methods
2017
28722025
Nanopore long-read RNAseq reveals widespread transcriptional variation among the surface receptors of individual B cells.
Nat Commun
2017
27887629
The Oxford Nanopore MinION: delivery of nanopore sequencing to the genomics community.
Genome Biol
2016
27964738
Erratum to: The Oxford Nanopore MinION: delivery of nanopore sequencing to the genomics community.
Genome Biol
2016
25686389
Improved data analysis for the MinION nanopore sequencer.
Nat Methods
2015
26834992
MinION Analysis and Reference Consortium: Phase 1 data release and analysis.
F1000Res
2015
24501022
Centromere reference models for human chromosomes X and Y satellite arrays.
Genome Res
2014
21964054
Cancer vaccines and carbohydrate epitopes.
Vaccine
2011
1 - 47 of 47
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