Cargando…

Author Correction: Searching thousands of genomes to classify somatic and novel structural variants using STIX

Detalles Bibliográficos
Autores principales:	Chowdhury, Murad, Pedersen, Brent S., Sedlazeck, Fritz J., Quinlan, Aaron R., Layer, Ryan M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group US 2022
Materias:	Author Correction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9184272/ https://www.ncbi.nlm.nih.gov/pubmed/35618956 http://dx.doi.org/10.1038/s41592-022-01538-8

Ejemplares similares

Searching thousands of genomes to classify somatic and novel structural variants using STIX
por: Chowdhury, Murad, et al.
Publicado: (2022)

Author Correction: Towards accurate and reliable resolution of structural variants for clinical diagnosis
por: Liu, Zhichao, et al.
Publicado: (2022)

SV-plaudit: A cloud-based framework for manually curating thousands of structural variants
por: Belyeu, Jonathan R, et al.
Publicado: (2018)

Samplot: a platform for structural variant visual validation and automated filtering
por: Belyeu, Jonathan R., et al.
Publicado: (2021)

Thomas H. Stix Symposium on Advances in Plasma Physics
por: Fisch, Nathaniel J
Publicado: (1994)

Vcfanno: fast, flexible annotation of genetic variants
por: Pedersen, Brent S., et al.
Publicado: (2016)

First Hard X-Ray Imaging Results by Solar Orbiter STIX
por: Massa, Paolo, et al.
Publicado: (2022)

Author Correction: Butler enables rapid cloud-based analysis of thousands of human genomes
por: Yakneen, Sergei, et al.
Publicado: (2023)

Author Correction: The impact of rare germline variants on human somatic mutation processes
por: Vali-Pour, Mischan, et al.
Publicado: (2023)

Clinical results of intradiscal hydrogel administration (GelStix) in lumbar degenerative disc disease
por: CEYLAN, Ayşegül, et al.
Publicado: (2019)

Author Correction: R-loop-forming Sequences Analysis in Thousands of Viral Genomes Identify A New Common Element in Herpesviruses
por: Wongsurawat, Thidathip, et al.
Publicado: (2020)

Author Correction: Retrospective analysis of somatic mutations and clonal hematopoiesis in astronauts
por: Brojakowska, Agnieszka, et al.
Publicado: (2022)

Author Correction: Patterns of somatic structural variation in human cancer genomes
por: Li, Yilong, et al.
Publicado: (2023)

Author Correction: Discovery and population genomics of structural variation in a songbird genus
por: Weissensteiner, Matthias H., et al.
Publicado: (2021)

Author Correction: The prognostic effects of somatic mutations in ER-positive breast cancer
por: Griffith, Obi L., et al.
Publicado: (2018)

Author Correction: Analyses of non-coding somatic drivers in 2,658 cancer whole genomes
por: Rheinbay, Esther, et al.
Publicado: (2023)

Author Correction: Generation of somatic mitochondrial DNA-replaced cells for mitochondrial dysfunction treatment
por: Maeda, Hideki, et al.
Publicado: (2021)

Author Correction: Generation of somatic mitochondrial DNA-replaced cells for mitochondrial dysfunction treatment
por: Maeda, Hideki, et al.
Publicado: (2021)

Author Correction: Gender specific somatic symptom burden and mortality risk in the general population
por: Atasoy, Seryan, et al.
Publicado: (2022)

Author Correction: Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer
por: Akdemir, Kadir C., et al.
Publicado: (2023)

Author Correction: Integrated targeted metabolomic and lipidomic analysis: A novel approach to classifying early cystic precursors to invasive pancreatic cancer
por: Gaiser, Rogier Aäron, et al.
Publicado: (2022)

Author Correction: Machine Learning Classifies Core and Outer Fucosylation of N-Glycoproteins Using Mass Spectrometry
por: Hwang, Heeyoun, et al.
Publicado: (2020)

Author Correction: Somatic mutations in facial skin from countries of contrasting skin cancer risk
por: King, Charlotte, et al.
Publicado: (2023)

cyvcf2: fast, flexible variant analysis with Python
por: Pedersen, Brent S, et al.
Publicado: (2017)

Author Correction: Whole rumen metagenome sequencing allows classifying and predicting feed efficiency and intake levels in cattle
por: Delgado, Beatriz, et al.
Publicado: (2020)

Author Correction: Targeted sequencing reveals the somatic mutation landscape in a Swedish breast cancer cohort
por: Mathioudaki, Argyri, et al.
Publicado: (2021)

Author Correction: Special vulnerability of somatic niche cells to transposable element activation in Drosophila larval ovaries
por: Sokolova, Olesya A., et al.
Publicado: (2021)

Author Correction: Deep learning versus human graders for classifying diabetic retinopathy severity in a nationwide screening program
por: Ruamviboonsuk, Paisan, et al.
Publicado: (2019)

Author Correction: A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns
por: Jiao, Wei, et al.
Publicado: (2022)

Interaction between somatic mutations and germline variants contributes to clinical heterogeneity in cancer
por: Musa, Julian, et al.
Publicado: (2019)

Duphold: scalable, depth-based annotation and curation of high-confidence structural variant calls
por: Pedersen, Brent S, et al.
Publicado: (2019)

Author Correction: 3D Muography for the Search of Hidden Cavities
por: Cimmino, Luigi, et al.
Publicado: (2019)

Author Correction: DNA damage and somatic mutations in mammalian cells after irradiation with a nail polish dryer
por: Zhivagui, Maria, et al.
Publicado: (2023)

Author Correction: Screening adequacy of unstained thyroid fine needle aspiration samples using a deep learning-based classifier
por: Jang, Junbong, et al.
Publicado: (2023)

Author Correction: Somatic mosaicism and common genetic variation contribute to the risk of very-early-onset inflammatory bowel disease
por: Serra, Eva Gonçalves, et al.
Publicado: (2022)

Author Directory
Publicado: (2013)

Author Index
Publicado: (2013)

Author Correction: Search and rescue at sea aided by hidden flow structures
por: Serra, Mattia, et al.
Publicado: (2020)

Author Correction: Viscoelastic properties of Pseudomonas aeruginosa variant biofilms
por: Gloag, Erin S., et al.
Publicado: (2022)

Author Correction: Inferring structural variant cancer cell fraction
por: Cmero, Marek, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_gn6f907uis9n2ua3kebr62v9o9