Results 191 to 200 of about 2,232,801 (311)
Omada: Robust clustering of transcriptomes through multiple testing
Kariotis S +6 more
europepmc +1 more source
Non-adjustment for multiple testing in multi-arm trials of distinct treatments: Rationale and justification. [PDF]
Parker RA, Weir CJ.
europepmc +1 more source
Intratumour heterogeneity complicates precision management of advanced endometrial cancer. Circulating tumor DNA (ctDNA) offers a minimally invasive strategy to capture tumor evolution and therapeutic resistance. Here, we compare tumor‐agnostic NGS with tumor‐informed ddPCR, outlining their relative sensitivity, concordance, and clinical implications ...
Carlos Casas‐Arozamena +15 more
wiley +1 more source
A new <i>p</i>-value based multiple testing procedure for generalized linear models. [PDF]
Rilling J, Tang CY.
europepmc +1 more source
Here, we demonstrate that HS1BP3 interacts with Cortactin through a proline‐rich region (PRR3.1) and show that this interaction, and HS1BP3 itself, promote cancer cell proliferation and invasion. Inhibition of this interaction leads to build‐up of TKS5 in multivesicular endosomes and altered secretion of CD63 and CD9, providing an explanation for the ...
Arja Arnesen Løchen +9 more
wiley +1 more source
A Novel BCR::ABL1 Variant Detected with Multiple Testing Modalities. [PDF]
Jean J +4 more
europepmc +1 more source
Circulating tumor cells (CTCs) and plasma cell‐free DNA (cfDNA) were analyzed to detect ESR1 mutations and methylation in patients with advanced breast cancer. CTC‐derived DNA showed higher sensitivity for mutation detection and revealed complementary genetic and epigenetic alterations, highlighting the added value of CTC analysis for understanding ...
Dimitra Stergiopoulou +12 more
wiley +1 more source
Combined multiple testing of multivariate survival times by censored empirical likelihood. [PDF]
Parkinson JH.
europepmc +1 more source
Interpreting the effects of DNA polymerase variants at the structural level
Using MAVISp and molecular dynamics simulations, we analyzed over 60 000 missense variants in POLE and POLD1 from ClinVar, COSMIC, cBioPortal, and saturation mutagenesis. Identified mechanistic indicators, including stability, binding, and long‐range, enable structural interpretation, providing ACMG‐like evidence for possible reclassification of VUS ...
Matteo Arnaudi +7 more
wiley +1 more source
The impact of allocation bias on test decisions in clinical trials with multiple endpoints using multiple testing strategies. [PDF]
Schoenen S +3 more
europepmc +1 more source

