Search Results - "Goodwin, Sara"
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Coming of age: ten years of next-generation sequencing technologies
Published in Nature reviews. Genetics (01-06-2016)“…Key Points There are two major paradigms in next-generation sequencing (NGS) technology: short-read sequencing and long-read sequencing. Short-read sequencing…”
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RaGOO: fast and accurate reference-guided scaffolding of draft genomes
Published in Genome Biology (28-10-2019)“…We present RaGOO, a reference-guided contig ordering and orienting tool that leverages the speed and sensitivity of Minimap2 to accurately achieve…”
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Oxford Nanopore sequencing, hybrid error correction, and de novo assembly of a eukaryotic genome
Published in Genome research (01-11-2015)“…Monitoring the progress of DNA molecules through a membrane pore has been postulated as a method for sequencing DNA for several decades. Recently, a…”
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Machine learning to predict occult nodal metastasis in early oral squamous cell carcinoma
Published in Oral oncology (01-05-2019)“…•Prediction of occult nodal metastasis can be used to guide surgical treatment.•Improved predictive methods may personalize treatment of early oral…”
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Complex rearrangements and oncogene amplifications revealed by long-read DNA and RNA sequencing of a breast cancer cell line
Published in Genome research (01-08-2018)“…The SK-BR-3 cell line is one of the most important models for HER2+ breast cancers, which affect one in five breast cancer patients. SK-BR-3 is known to be…”
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Comprehensive analysis of structural variants in breast cancer genomes using single-molecule sequencing
Published in Genome research (01-09-2020)“…Improved identification of structural variants (SVs) in cancer can lead to more targeted and effective treatment options as well as advance our basic…”
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High resolution copy number inference in cancer using short-molecule nanopore sequencing
Published in Nucleic acids research (02-12-2021)“…Abstract Genome copy number is an important source of genetic variation in health and disease. In cancer, Copy Number Alterations (CNAs) can be inferred from…”
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Gene recoding by synonymous mutations creates promiscuous intragenic transcription initiation in mycobacteria
Published in mBio (31-10-2023)“…( ) is the causative agent of tuberculosis, one of the deadliest infectious diseases worldwide. Previous studies have established that synonymous recoding to…”
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Transcriptional Silencing of ALDH2 Confers a Dependency on Fanconi Anemia Proteins in Acute Myeloid Leukemia
Published in Cancer discovery (01-09-2021)“…Hundreds of genes become aberrantly silenced in acute myeloid leukemia (AML), with most of these epigenetic changes being of unknown functional consequence…”
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MinION Analysis and Reference Consortium: Phase 1 data release and analysis
Published in F1000 research (2015)“…The advent of a miniaturized DNA sequencing device with a high-throughput contextual sequencing capability embodies the next generation of large scale…”
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Whole Genome Sequencing and Assembly of the Asian Honey Bee Apis dorsata
Published in Genome biology and evolution (01-01-2020)“…Abstract The Asian honey bee (Apis dorsata) is distinct from its more widely distributed cousin Apis mellifera by a few key characteristics. Most prominently,…”
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Associations between circulating interferon and kynurenine/tryptophan pathway metabolites: support for a novel potential mechanism for cognitive dysfunction in SLE
Published in Lupus science & medicine (01-11-2022)“…ObjectiveQuinolinic acid (QA), a kynurenine (KYN)/tryptophan (TRP) pathway metabolite, is an N-methyl-D-aspartate receptor agonist that can produce excitotoxic…”
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621 The Association of Interferon with Kynurenine/Tryptophan Pathway Activation in Systemic Lupus Erythematosus
Published in Lupus science & medicine (14-12-2022)“…BackgroundCognitive dysfunction (CD) is highly prevalent in systemic lupus erythematosus (SLE) with significant impact on quality of life, yet SLE-mediated…”
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Management, Analyses, and Distribution of the MaizeCODE Data on the Cloud
Published in Frontiers in plant science (31-03-2020)“…MaizeCODE is a project aimed at identifying and analyzing functional elements in the maize genome. In its initial phase, MaizeCODE assayed up to five tissues…”
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Next-Generation Sequencing as Input for Chemometrics in Differential Sensing Routines
Published in Angewandte Chemie International Edition (18-05-2015)“…Differential sensing (DS) methods traditionally use spatially arrayed receptors and optical signals to create score plots from multivariate data which classify…”
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Abstract 5136: Adapting long read sequencing technologies for targeted and single cell applications
Published in Cancer research (Chicago, Ill.) (01-07-2019)“…Abstract Structural variations (SV), a hallmark of genomic instability in cancer, include insertions, deletions, duplications, inversions, or translocations…”
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Abstract LB201: Understanding genetic variation in cancer using nanopore targeted sequencing
Published in Cancer research (Chicago, Ill.) (01-07-2021)“…Abstract Structural variations (SV), a hallmark of genomic instability in cancer can either activate oncogenes or inactivate tumor suppressor genes. SVs tend…”
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Era of gapless plant genomes: innovations in sequencing and mapping technologies revolutionize genomics and breeding
Published in Current opinion in biotechnology (01-02-2023)“…Whole-genome sequencing and assembly have revolutionized plant genetics and molecular biology over the last two decades. However, significant shortcomings in…”
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Major Impacts of Widespread Structural Variation on Gene Expression and Crop Improvement in Tomato
Published in Cell (09-07-2020)“…Structural variants (SVs) underlie important crop improvement and domestication traits. However, resolving the extent, diversity, and quantitative impact of…”
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Abstract 1360: Understanding genetic variation in cancer using targeted nanopore long read sequencing
Published in Cancer research (Chicago, Ill.) (15-08-2020)“…Abstract Structural variations (SV), a hallmark of genomic instability in cancer can either activate oncogenes or inactivate tumor suppressor genes. SVs tend…”
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