Detalhe da pesquisa
1.
Single-cell transcriptomics reconstructs fate conversion from fibroblast to cardiomyocyte.
Nature
; 551(7678): 100-104, 2017 11 02.
Artigo
Inglês
| MEDLINE | ID: mdl-29072293
2.
Deep sequencing shows multiple oligouridylations are required for 3' to 5' degradation of histone mRNAs on polyribosomes.
Mol Cell
; 53(6): 1020-30, 2014 Mar 20.
Artigo
Inglês
| MEDLINE | ID: mdl-24656133
3.
Robust detection of alternative splicing in a population of single cells.
Nucleic Acids Res
; 44(8): e73, 2016 05 05.
Artigo
Inglês
| MEDLINE | ID: mdl-26740580
4.
Selective single cell isolation for genomics using microraft arrays.
Nucleic Acids Res
; 44(17): 8292-301, 2016 09 30.
Artigo
Inglês
| MEDLINE | ID: mdl-27530426
5.
Variation in chromatin accessibility in human kidney cancer links H3K36 methyltransferase loss with widespread RNA processing defects.
Genome Res
; 24(2): 241-50, 2014 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-24158655
6.
EnD-Seq and AppEnD: sequencing 3' ends to identify nontemplated tails and degradation intermediates.
RNA
; 21(7): 1375-89, 2015 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-26015596
7.
Pseudogenes transcribed in breast invasive carcinoma show subtype-specific expression and ceRNA potential.
BMC Genomics
; 16: 113, 2015 Feb 22.
Artigo
Inglês
| MEDLINE | ID: mdl-25765044
8.
BlackOPs: increasing confidence in variant detection through mappability filtering.
Nucleic Acids Res
; 41(19): e178, 2013 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-23935067
9.
DiffSplice: the genome-wide detection of differential splicing events with RNA-seq.
Nucleic Acids Res
; 41(2): e39, 2013 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-23155066
10.
FDM: a graph-based statistical method to detect differential transcription using RNA-seq data.
Bioinformatics
; 27(19): 2633-40, 2011 Oct 01.
Artigo
Inglês
| MEDLINE | ID: mdl-21824971
11.
MapSplice: accurate mapping of RNA-seq reads for splice junction discovery.
Nucleic Acids Res
; 38(18): e178, 2010 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-20802226
12.
NeoSplice: a bioinformatics method for prediction of splice variant neoantigens.
Bioinform Adv
; 2(1): vbac032, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-35669345
13.
A probabilistic framework for aligning paired-end RNA-seq data.
Bioinformatics
; 26(16): 1950-7, 2010 Aug 15.
Artigo
Inglês
| MEDLINE | ID: mdl-20576625
14.
Single-Cell Transcriptomic Analyses of Cell Fate Transitions during Human Cardiac Reprogramming.
Cell Stem Cell
; 25(1): 149-164.e9, 2019 07 03.
Artigo
Inglês
| MEDLINE | ID: mdl-31230860
15.
MATCHER: manifold alignment reveals correspondence between single cell transcriptome and epigenome dynamics.
Genome Biol
; 18(1): 138, 2017 07 24.
Artigo
Inglês
| MEDLINE | ID: mdl-28738873
16.
SLICER: inferring branched, nonlinear cellular trajectories from single cell RNA-seq data.
Genome Biol
; 17(1): 106, 2016 05 23.
Artigo
Inglês
| MEDLINE | ID: mdl-27215581
17.
Cache-Aware Asymptotically-Optimal Sampling-Based Motion Planning.
IEEE Int Conf Robot Autom
; 2014: 5804-5810, 2014 May.
Artigo
Inglês
| MEDLINE | ID: mdl-25419474
18.
A robust method for transcript quantification with RNA-seq data.
J Comput Biol
; 20(3): 167-87, 2013 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-23461570