Transcriptome Sequencing Reveals Potential Mechanism of Cryptic 3’ Splice Site Selection in SF3B1-mutated Cancers

The Cancer Genomics Hub (CGHub): overcoming cancer through the power of torrential data

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SF3B1 mutations in chronic lymphocytic leukemia

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Subclonal evolution involving SF3B1 mutations in chronic lymphocytic leukemia

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Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3

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Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanoma

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STAR: ultrafast universal RNA-seq aligner

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Detecting differential usage of exons from RNA-seq data

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Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes

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SCFFbxo9 and CK2 direct the cellular response to growth factor withdrawal via Tel2/Tti1 degradation and promote survival in multiple myeloma

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Streaming fragment assignment for real-time analysis of sequencing experiments

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Fast gapped-read alignment with Bowtie 2

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New connections between splicing and human disease

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Integrative annotation of human large intergenic noncoding RNAs reveals global properties and specific subclasses

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Frequent pathway mutations of splicing machinery in myelodysplasia

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Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia

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SomaticSF3B1Mutation in Myelodysplasia with Ring Sideroblasts

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SF3B1and Other Novel Cancer Genes in Chronic Lymphocytic Leukemia

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A genetic screen identifies the Triple T complex required for DNA damage signaling and ATM and ATR stability

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Tti1 and Tel2 Are Critical Factors in Mammalian Target of Rapamycin Complex Assembly

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COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer

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Genome-Wide Association between Branch Point Properties and Alternative Splicing

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Differential expression analysis for sequence count data

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H-InvDB in 2009: extended database and data mining resources for human genes and transcripts

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Human branch point consensus sequence is yUnAy

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