Search Results - "Frankish, Adam"

Genetic Data: Potential Uses and Misuses in Marketing.

Authors: Daviet, Remi Nave, Gideon Wind, Jerry

Source: Journal of Marketing. Jan2022, Vol. 86 Issue 1, p7-26. 20p. 2 Diagrams, 2 Charts.

Multiomics integration unravels genotype‐microbiome interactions shaping the conjunctival transcriptome.

Authors: Liang, Qiaoxing Lin, Guo‐Wang Ding, Xiaohu et al.

Source: iMetaOmics. Dec2024, Vol. 1 Issue 2, p1-15. 15p.

The value of primary transcripts to the clinical and non‐clinical genomics community: Survey results and roadmap for improvements.

Authors: Morales, Joannella McMahon, Aoife C. Loveland, Jane et al.

Source: Molecular Genetics & Genomic Medicine. Dec2021, Vol. 9 Issue 12, p1-8. 8p.

Non‐coding regulatory elements: Potential roles in disease and the case of epilepsy.

Authors: Pagni, Susanna Mills, James D. Frankish, Adam et al.

Source: Neuropathology & Applied Neurobiology. Apr2022, Vol. 48 Issue 3, p1-20. 20p.

A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes.

Authors: MacArthur, Daniel G. Balasubramanian, Suganthi Frankish, Adam et al.

Source: Science (pre-March 2025). 2/17/2012, Vol. 335 Issue 6070, p823-828. 6p.

Comparison of GENCODE and RefSeq gene annotation and the impact of reference geneset on variant effect prediction.

Authors: Frankish, Adam Uszczynska, Barbara Ritchie, Graham R. S. et al.

Source: BMC Genomics. 2015 Suppl 8, Vol. 16, p1-11. 11p. 1 Diagram, 1 Chart, 3 Graphs.

The DNA sequence of the human X chromosome.

Authors: Ross, Mark T. Grafham, Darren V. Coffey, Alison J. et al.

Source: Nature. 3/17/2005, Vol. 434 Issue 7031, p325-337. 13p.

Subjects: Nucleotide sequence, X chromosome, Sex chromosomes, Human genome, Genes, Genetics, Human genetics

Evidence for a novel overlapping coding sequence in POLG initiated at a CUG start codon.

Authors: Khan, Yousuf A. Jungreis, Irwin Wright, James C. et al.

Source: BMC Genetics. 3/6/2020, Vol. 21 Issue 1, p1-16. 16p.

Expert curation of the human and mouse olfactory receptor gene repertoires identifies conserved coding regions split across two exons.

Authors: Barnes, If H. A. Ibarra-Soria, Ximena Fitzgerald, Stephen et al.

Source: BMC Genomics. 3/3/2020, Vol. 21 Issue 1, p1-15. 15p. 1 Diagram, 3 Charts, 4 Graphs.

ISOGO: Functional annotation of protein-coding splice variants.

Authors: Ferrer-Bonsoms, Juan A Cassol, Ignacio Fernández-Acín, Pablo et al.

Source: Scientific Reports. 1/23/2020, Vol. 10 Issue 1, p1-11. 11p.

A deep neural network approach to predicting clinical outcomes of neuroblastoma patients.

Authors: Tranchevent, Léon-Charles Azuaje, Francisco Rajapakse, Jagath C.

Source: BMC Medical Genomics. 12/20/2019 Supplement 8, Vol. 12, p1-11. 11p.

Genome annotation for clinical genomic diagnostics: strengths and weaknesses.

Authors: Steward, Charles A. Parker, Alasdair P. J. Minassian, Berge A. et al.

Source: Genome Medicine. 5/30/2017, Vol. 9, p1-19. 19p.

Efficient targeted transcript discovery via array-based normalization of RACE libraries.

Authors: Djebali, Sarah Kapranov, Philipp Foissac, Sylvain et al.

Source: Nature Methods. Jul2008, Vol. 5 Issue 7, p629-635. 7p. 2 Diagrams, 1 Chart, 3 Graphs.

Polymorphic segmental duplications at 8p23.1 challenge the determination of individual defensin gene repertoires and the assembly of a contiguous human reference sequence.

Authors: Taudien, Stefan Galgoczy, Petra Huse, Klaus et al.

Source: BMC Genomics. 2004, Vol. 5, p92-12. 12p. 3 Diagrams, 2 Charts.

Hidden Markov models lead to higher resolution maps of mutation signature activity in cancer.

Authors: Wojtowicz, Damian Sason, Itay Huang, Xiaoqing et al.

Source: Genome Medicine. 7/26/2019, Vol. 11 Issue 1, pN.PAG-N.PAG. 1p.

Retroposed copies of RET gene: a somatically acquired event in medullary thyroid carcinoma.

Authors: Bim, Larissa V. Navarro, Fábio C. P. Valente, Flávia O. F. et al.

Source: BMC Medical Genomics. 7/9/2019, Vol. 12 Issue 1, pN.PAG-N.PAG. 1p.

Evolutionary history of the human multigene families reveals widespread gene duplications throughout the history of animals.

Authors: Pervaiz, Nashaiman Shakeel, Nazia Qasim, Ayesha et al.

Source: BMC Evolutionary Biology. 6/20/2019, Vol. 19 Issue 1, pN.PAG-N.PAG. 1p.

Screening for mouse genes lost in mammals with long lifespans.

Authors: Rubanov, Lev I. Zaraisky, Andrey G. Shilovsky, Gregory A. et al.

Source: BioData Mining. 11/9/2019, Vol. 12 Issue 1, pN.PAG-N.PAG. 1p.

A purely bioinformatic pipeline for the prediction of mammalian odorant receptor gene enhancers.

Authors: Degl'Innocenti, Andrea Meloni, Gabriella Mazzolai, Barbara et al.

Source: BMC Bioinformatics. 9/14/2019, Vol. 20 Issue 1, pN.PAG-N.PAG. 1p. 1 Diagram, 2 Charts, 4 Graphs.

deSALT: fast and accurate long transcriptomic read alignment with de Bruijn graph-based index.

Authors: Liu B Liu Y Li J et al.

Source: Genome biology [Genome Biol] 2019 Dec 16; Vol. 20 (1), pp. 274. Date of Electronic Publication: 2019 Dec 16.

Publication Type: Evaluation Study; Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: BioMed Central Ltd Country of Publication: England NLM ID: 100960660 Publication Model: Electronic Cited Medium: Internet ISSN: 1474-760X (Electronic) Linking ISSN: 14747596 NLM ISO Abbreviation: Genome Biol Subsets: MEDLINE