Suchergebnisse - "CMM Groep De Ridder"

Author Correction: Accurate detection of circulating tumor DNA using nanopore consensus sequencing (npj Genomic Medicine, (2021), 6, 1, (106), 10.1038/s41525-021-00272-y)

Autoren: CMM Groep De Ridder Cancer Genetica Medische Informatica et al.

URL: https://doi.org/10.1038/s41525-023-00356-x
http://hdl.handle.net/1874/449348
https://dspace.library.uu.nl/handle/1874/449348
http://www.scopus.com/inward/record.url?scp=85161018404&partnerID=8YFLogxK
2056-7944
npj Genomic Medicine
8
1
12

Author Correction: A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns (Nature Communications, (2020), 11, 1, (728), 10.1038/s41467-019-13825-8)

Autoren: CMM Groep Cuppen Cancer CMM et al.

URL: https://doi.org/10.1038/s41467-022-32329-6
http://hdl.handle.net/1874/453958
https://dspace.library.uu.nl/handle/1874/453958
http://www.scopus.com/inward/record.url?scp=85143564414&partnerID=8YFLogxK
2041-1723
Nature Communications
13
1
7573

Author Correction: A replication study of genetic risk loci for ischemic stroke in a Dutch population: a case-control study

Autoren: Brain CMM Groep De Ridder Circulatory Health et al.

URL: https://doi.org/10.1038/s41598-018-22952-z
http://hdl.handle.net/1874/363802
2045-2322
Scientific Reports
8
1
6057

Eleven grand challenges in single-cell data science

Autoren: Hubrecht Institute with UMC CMM Groep De Ridder Cancer et al.

URL: https://doi.org/10.1186/s13059-020-1926-6
http://hdl.handle.net/1874/442199
http://www.scopus.com/inward/record.url?scp=85079082934&partnerID=8YFLogxK
1465-6906
Genome Biology
21
1
1
35
31

Author Correction: Accurate detection of circulating tumor DNA using nanopore consensus sequencing (npj Genomic Medicine, (2021), 6, 1, (106), 10.1038/s41525-021-00272-y)

Autoren: Marcozzi, Alessio Jager, Myrthe Elferink, Martin et al.

Weitere Verfasser: Marcozzi, Alessio Jager, Myrthe Elferink, Martin et al.

Schlagwörter: Published Erratum

Dateibeschreibung: application/pdf

Relation: https://dspace.library.uu.nl/handle/1874/449348

Verfügbarkeit: https://dspace.library.uu.nl/handle/1874/449348

Author Correction: A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns (Nature Communications, (2020), 11, 1, (728), 10.1038/s41467-019-13825-8)

Autoren: Jiao, Wei Atwal, Gurnit Polak, Paz et al.

Weitere Verfasser: Jiao, Wei Atwal, Gurnit Polak, Paz et al.

Schlagwörter: General Chemistry, General Biochemistry,Genetics and Molecular Biology, General Physics and Astronomy

Dateibeschreibung: application/pdf

Relation: https://dspace.library.uu.nl/handle/1874/453958

Verfügbarkeit: https://dspace.library.uu.nl/handle/1874/453958

Eleven grand challenges in single-cell data science

Autoren: all co-authors Hubrecht Institute with UMC CMM Groep De Ridder et al.

Weitere Verfasser: all co-authors Hubrecht Institute with UMC CMM Groep De Ridder et al.

Schlagwörter: Animals, Data Science/methods, Genomics/methods, Humans, RNA-Seq/methods, Single-Cell Analysis/methods, Genetics, Ecology, Evolution, Behavior and Systematics, Cell Biology, Review, Research Support, Non-U.S. Gov't, U.S. Gov't, Non-P.H.S, Journal Article, N.I.H., Extramural

Dateibeschreibung: application/pdf

Relation: https://dspace.library.uu.nl/handle/1874/442199

Verfügbarkeit: https://dspace.library.uu.nl/handle/1874/442199

ECCB 2016: The 15th European Conference on Computational Biology: The 15th European Conference on Computational Biology

Autoren: Heringa, Jaap (author) Reinders, M.J.T. (author) Abeln, Sanne (author) et al.

Weitere Verfasser: Heringa, Jaap (author) Reinders, M.J.T. (author) Abeln, Sanne (author) et al.

Quelle: Bioinformatics. 32:i389-i392

Schlagwörter: Statistics and Probability, 0301 basic medicine, Computational Mathematics, 03 medical and health sciences, Editorial, Computational Theory and Mathematics, 0206 medical engineering, General Medicine, 02 engineering and technology, Biochemistry, Molecular Biology, Computer Science Applications

Dateibeschreibung: application/pdf

Zugangs-URL: https://academic.oup.com/bioinformatics/article-pdf/32/17/i389/24151517/btw481.pdf
https://pubmed.ncbi.nlm.nih.gov/27587653
https://research.vu.nl/en/publications/d59c18ad-b301-43e6-91ae-bb2ef46f7657
https://hdl.handle.net/1871.1/d59c18ad-b301-43e6-91ae-bb2ef46f7657
https://doi.org/10.1093/bioinformatics/btw481
https://dspace.library.uu.nl/handle/1874/354205

Author Correction: A replication study of genetic risk loci for ischemic stroke in a Dutch population: a case-control study

Autoren: Hauer, Allard J Pulit, Sara L van den Berg, Leonard H et al.

Weitere Verfasser: Hauer, Allard J Pulit, Sara L van den Berg, Leonard H et al.

Schlagwörter: Published Erratum

Dateibeschreibung: image/pdf

Relation: https://dspace.library.uu.nl/handle/1874/363802

Verfügbarkeit: https://dspace.library.uu.nl/handle/1874/363802

Integrated clinical and omics approach to rare diseases: novel genes and oligogenic inheritance in holoprosencephaly: novel genes and oligogenic inheritance in holoprosencephaly

Autoren: Artem Kim Clara Savary Christèle Dubourg et al.

Weitere Verfasser: Artem Kim Clara Savary Christèle Dubourg et al.

Quelle: Brain. 142:35-49

Schlagwörter: EXPRESSION, Exome/genetics, Male, 0301 basic medicine, Multifactorial Inheritance, Holoprosencephaly/genetics, Clinical Neurology, [SDV.GEN] Life Sciences [q-bio]/Genetics, MICE LACKING, MOUSE, PHENOTYPE, GUIDELINES, PATHWAY, sonic hedgehog, 03 medical and health sciences, primary cilia, DEFICIENT, Rare Diseases/genetics, Rare Diseases, Holoprosencephaly, SEQUENCE VARIANTS, Humans, oligogenic inheritance, Exome, [SDV.NEU] Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC], Multifactorial Inheritance/genetics, [SDV.GEN]Life Sciences [q-bio]/Genetics, Comparative Genomic Hybridization, 0303 health sciences, IDENTIFICATION, MUTATIONS, Pedigree, 3. Good health, holoprosencephaly, Phenotype, Case-Control Studies, Mutation, [SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC], Female, exome

Dateibeschreibung: application/pdf

Zugangs-URL: https://academic.oup.com/brain/article-pdf/142/1/35/27497908/awy290.pdf
https://pubmed.ncbi.nlm.nih.gov/30508070
https://research.rug.nl/en/publications/integrated-clinical-and-omics-approach-to-rare-diseases-novel-gen
https://academic.oup.com/brain/article/142/1/35/5224997
http://dspace.library.uu.nl/handle/1874/392174
https://hal.archives-ouvertes.fr/hal-01975696
https://www.cardioscience.ox.ac.uk/publications/982604
https://pubmed.ncbi.nlm.nih.gov/30508070/
https://www.biorxiv.org/content/early/2018/05/11/320127
https://www.biorxiv.org/content/10.1101/320127v1
https://www.biorxiv.org/content/10.1101/320127v1.article-metrics
https://www.biorxiv.org/content/biorxiv/early/2018/05/11/320127.full.pdf
https://dspace.library.uu.nl/handle/1874/392174