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Titlebook: Cancer Genomics and Proteomics; Methods and Protocol Narendra Wajapeyee Book 2014Latest edition Springer Science+Business Media New York 20

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樓主: SPARK
31#
發(fā)表于 2025-3-26 21:36:26 | 只看該作者
Vladimir Kanchev,Roumen Kountcheval methods that use exome sequencing reads from cancer samples to identify somatic single nucleotide variants (SNVs), copy number alterations, and short insertions and deletions (InDels). We further describe analytical methods to generate lists of driver genes with more mutational events than expect
32#
發(fā)表于 2025-3-27 04:17:44 | 只看該作者
33#
發(fā)表于 2025-3-27 07:47:30 | 只看該作者
Cancer Genomics and Proteomics978-1-4939-0992-6Series ISSN 1064-3745 Series E-ISSN 1940-6029
34#
發(fā)表于 2025-3-27 12:04:19 | 只看該作者
35#
發(fā)表于 2025-3-27 16:48:41 | 只看該作者
New Approaches in Intelligent Controlification arise when proteins are of low abundance or are unstable resulting in low yields or poor in vitro activity. In this protocol we describe a method to purify active, recombinant human proteins fused to a tandem MBP tag after expression in human 293T cells.
36#
發(fā)表于 2025-3-27 18:48:23 | 只看該作者
37#
發(fā)表于 2025-3-27 23:11:02 | 只看該作者
https://doi.org/10.1007/978-1-4939-0992-6cancer cells; cancer genome; genome; progression; proteome; transcriptome; tumor cells; tumor initiation; Pr
38#
發(fā)表于 2025-3-28 05:19:34 | 只看該作者
978-1-4939-4654-9Springer Science+Business Media New York 2014
39#
發(fā)表于 2025-3-28 06:45:57 | 只看該作者
Targeted Genome Modification via Triple Helix Formation,en coordinating homologous recombination events. Here, we describe the use of TFOs such as peptide nucleic acids for targeted genome modification. We discuss this method and its applications and describe protocols for TFO design, delivery, and evaluation of activity in vitro and in vivo.
40#
發(fā)表于 2025-3-28 14:20:55 | 只看該作者
Purification of Recombinant 2XMBP Tagged Human Proteins from Human Cells,ification arise when proteins are of low abundance or are unstable resulting in low yields or poor in vitro activity. In this protocol we describe a method to purify active, recombinant human proteins fused to a tandem MBP tag after expression in human 293T cells.
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