Detalhe da pesquisa
1.
Pan-cancer genome and transcriptome analyses of 1,699 paediatric leukaemias and solid tumours.
Nature
; 555(7696): 371-376, 2018 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29489755
2.
Cancer germline predisposing variants and late mortality from subsequent malignant neoplasms among long-term childhood cancer survivors: a report from the St Jude Lifetime Cohort and the Childhood Cancer Survivor Study.
Lancet Oncol
; 24(10): 1147-1156, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37797633
3.
indelPost: harmonizing ambiguities in simple and complex indel alignments.
Bioinformatics
; 38(2): 549-551, 2022 01 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34431982
4.
Pediatric Cancer Variant Pathogenicity Information Exchange (PeCanPIE): a cloud-based platform for curating and classifying germline variants.
Genome Res
; 29(9): 1555-1565, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31439692
5.
Therapy-induced mutations drive the genomic landscape of relapsed acute lymphoblastic leukemia.
Blood
; 135(1): 41-55, 2020 01 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31697823
6.
RNAIndel: discovering somatic coding indels from tumor RNA-Seq data.
Bioinformatics
; 36(5): 1382-1390, 2020 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31593214
7.
The landscape of coding RNA editing events in pediatric cancer.
BMC Cancer
; 21(1): 1233, 2021 Nov 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-34789196
8.
Inhibition of SF3B1 by molecules targeting the spliceosome results in massive aberrant exon skipping.
RNA
; 24(8): 1056-1066, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29844105
9.
Germline Mutations in Predisposition Genes in Pediatric Cancer.
N Engl J Med
; 373(24): 2336-2346, 2015 Dec 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-26580448
10.
RNAIndel: discovering somatic coding indels from tumor RNA-Seq data.
Bioinformatics
; 36(14): 4231, 2020 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-32572447
11.
Corrigendum: Inhibition of SF3B1 by molecules targeting the spliceosome results in massive aberrant exon skipping.
RNA
; 24(12): 1886, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30446591
12.
Defining the condensate landscape of fusion oncoproteins.
Nat Commun
; 14(1): 6008, 2023 09 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-37770423
13.
Bambino: a variant detector and alignment viewer for next-generation sequencing data in the SAM/BAM format.
Bioinformatics
; 27(6): 865-6, 2011 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21278191
14.
Exploration of Coding and Non-coding Variants in Cancer Using GenomePaint.
Cancer Cell
; 39(1): 83-95.e4, 2021 01 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33434514
15.
Genomes for Kids: The Scope of Pathogenic Mutations in Pediatric Cancer Revealed by Comprehensive DNA and RNA Sequencing.
Cancer Discov
; 11(12): 3008-3027, 2021 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34301788
16.
St. Jude Cloud: A Pediatric Cancer Genomic Data-Sharing Ecosystem.
Cancer Discov
; 11(5): 1082-1099, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33408242
17.
Shortened Leukocyte Telomere Length Associates with an Increased Prevalence of Chronic Health Conditions among Survivors of Childhood Cancer: A Report from the St. Jude Lifetime Cohort.
Clin Cancer Res
; 26(10): 2362-2371, 2020 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31969337
18.
Pathogenic Germline Mutations in DNA Repair Genes in Combination With Cancer Treatment Exposures and Risk of Subsequent Neoplasms Among Long-Term Survivors of Childhood Cancer.
J Clin Oncol
; 38(24): 2728-2740, 2020 08 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-32496904
19.
CICERO: a versatile method for detecting complex and diverse driver fusions using cancer RNA sequencing data.
Genome Biol
; 21(1): 126, 2020 05 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-32466770
20.
Discovery of regulatory noncoding variants in individual cancer genomes by using cis-X.
Nat Genet
; 52(8): 811-818, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32632335