Genomic Localization of a SMAD 4 Processed Pseudogene
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Laura A. Crinnion | A. Markham | A. Antanaviciute | I. Carr | J. Adlard | R. Charlton | N. Camm | C. Watson | T. David | Bonthron
[1] M. Mann,et al. SCAI promotes DNA double-strand break repair in distinct chromosomal contexts , 2016, Nature Cell Biology.
[2] E. Lyon,et al. Processed Pseudogene Confounding Deletion/Duplication Assays for SMAD4. , 2015, The Journal of molecular diagnostics : JMD.
[3] Ming Liu,et al. MiR-1228 promotes breast cancer cell growth and metastasis through targeting SCAI protein. , 2015, International journal of clinical and experimental pathology.
[4] Aung Ko Win,et al. PMS2 monoallelic mutation carriers: the known unknown , 2015, Genetics in Medicine.
[5] Lachlan James M. Coin,et al. cnvOffSeq: detecting intergenic copy number variation using off-target exome sequencing data , 2014, Bioinform..
[6] Matthew D. Wilkerson,et al. ABRA: improved coding indel detection via assembly-based realignment , 2014, Bioinform..
[7] Dirk Roos,et al. Primary Immunodeficiency Caused by an Exonized Retroposed Gene Copy Inserted in the CYBB Gene , 2014, Human mutation.
[8] Matthew W. Hahn,et al. Gene Copy-Number Polymorphism Caused by Retrotransposition in Humans , 2013, PLoS genetics.
[9] J. Long,et al. Exome sequencing generates high quality data in non-target regions , 2012, BMC Genomics.
[10] Helga Thorvaldsdóttir,et al. Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration , 2012, Briefings Bioinform..
[11] Christopher A. Miller,et al. VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. , 2012, Genome research.
[12] Marcel Martin. Cutadapt removes adapter sequences from high-throughput sequencing reads , 2011 .
[13] M. DePristo,et al. A framework for variation discovery and genotyping using next-generation DNA sequencing data , 2011, Nature Genetics.
[14] Eamonn Sheridan,et al. Genetic diagnosis of familial breast cancer using clonal sequencing , 2010, Human mutation.
[15] Thomas R. Gingeras,et al. STAR: ultrafast universal RNA-seq aligner , 2013, Bioinform..