Results 11 to 20 of about 600,345 (283)

Referee report. For: Evaluating the performance of tools used to call minority variants from whole genome short-read data [version 2; referees: 2 approved]

, 2018
Brad Chapman
openalex   +2 more sources

Referee report. For: Evaluating the performance of tools used to call minority variants from whole genome short-read data [version 1; referees: 1 approved with reservations]

, 2018
Brad Chapman
openalex   +2 more sources

Referee report. For: The genome sequence of the short-fringed mining bee, Andrena dorsata (Kirby, 1802) [version 1; peer review: 1 approved]

Manee M. Manee
openalex   +2 more sources

Referee report. For: Negligible effects of read trimming on the accuracy of germline short variant calling in the human genome [version 1; peer review: 2 approved with reservations]

Xihao Li, Muqing Zhou
openalex   +2 more sources

Short Report: Early genomic detection of SARS-CoV-2 P.1 variant in Northeast Brazil

PLOS Neglected Tropical Diseases, 2021
Tracking the spread of SARS-CoV-2 variants of concern is crucial to inform public health efforts and control the ongoing pandemic. Here, we report genetic evidence for circulation of the P.1 variant in Northeast Brazil. We advocate for increased active surveillance to ensure adequate control of this variant throughout the country.
Stephane Tosta, Marta Giovanetti, Vanessa Brandão Nardy, Luciana Reboredo de Oliveira da Silva, Marcela Kelly Astete Gómez, Jaqueline Gomes Lima, Cristiane Wanderley Cardoso, Tarcisio Oliveira Silva, Marcia São Pedro Leal de Souza, Pedro Henrique Presta Dia, Vagner Fonseca, Tulio de Oliveira, José Lourenço, Luiz Carlos Junior Alcantara, Felicidade Pereira, Arabela Leal   +15 more
openaire   +5 more sources

Referee report. For: Lessons learned: overcoming common challenges in reconstructing the SARS-CoV-2 genome from short-read sequencing data via CoVpipe2 [version 1; peer review: 1 approved, 1 approved with reservations]

S Boubaker
openalex   +2 more sources

Referee report. For: Negligible effects of read trimming on the accuracy of germline short variant calling in the human genome [version 1; peer review: 1 approved with reservations]

Dharma Varapula
openalex   +2 more sources

Correction: Short Report: Early genomic detection of SARS-CoV-2 P.1 variant in Northeast Brazil

PLOS Neglected Tropical Diseases, 2022
[This corrects the article DOI: 10.1371/journal.pntd.0009591.].
Stephane Tosta, Marta Giovanetti, Vanessa Brandão Nardy, Luciana Reboredo de Oliveira da Silva, Marcela Kelly Astete Gómez, Jaqueline Gomes Lima, Cristiane Wanderley Cardoso, Tarcisio Oliveira Silva, Marcia São Pedro Leal de Souza, Pedro Henrique Presta Dias, Vagner Fonseca, Tulio de Oliveira, José Lourenço, Luiz Carlos Junior Alcantara, Felicidade Pereira, Arabela Leal   +15 more
openaire   +2 more sources

FGF/FGFR genomic amplification as a predictive biomarker for immune checkpoint blockade resistance: a short report

Journal for ImmunoTherapy of Cancer, 2023
A novel crosstalk between immunogenic and oncometabolic pathways triggered by T cell-released interferon-gamma (IFN-ɣ) has been recently identified. This IFN-ɣ-pyruvate kinase M2-β-catenin axis relies on fibroblast growth factor 2 (FGF2) signaling in tumor cells and leads to hyperprogressive disease on immune checkpoint blockade (ICB) in preclinical ...
Nicolas Roussot, Julie Lecuelle, Lorraine Dalens, Caroline Truntzer, Francois Ghiringhelli   +4 more
openaire   +3 more sources

Proteomics and genomics of a monomorphic epitheliotropic intestinal T-cell lymphoma: An extremely rare case report and short review of literature

Medicine, 2022
Rationale: Monomorphic epitheliotropic intestinal T-cell lymphoma, formerly known as enteropathy-associated T-cell lymphoma, is an extremely rare, aggressive peripheral extranodal T-cell lymphoma, that is infrequent in native European and Caucasian populations.
Mădălina Boșoteanu, Miruna Cristian, Mariana Așchie, Mariana Deacu, Anca Florentina Mitroi, Costel Stelian Brînzan, Gabriela Izabela Bălțătescu   +6 more
openaire   +2 more sources