Confound
发表于 2025-3-25 04:13:15
,The Great War over Children, 1914–1918,e to quickly define all the insertional mutants in a library and thus identify nonessential genes under the conditions in which the library was produced. Identification of fitness of individual mutants under specific conditions can be performed by exposing the library to selective pressures.
justify
发表于 2025-3-25 08:25:00
http://reply.papertrans.cn/39/3820/381915/381915_22.png
脖子
发表于 2025-3-25 11:49:52
http://reply.papertrans.cn/39/3820/381915/381915_23.png
圆锥体
发表于 2025-3-25 17:25:08
http://reply.papertrans.cn/39/3820/381915/381915_24.png
暗语
发表于 2025-3-25 23:10:04
Gene Essentiality Analysis Based on DEG 10, an Updated Database of Essential Genes,ntial genes in bacterial genomes exhibits an exponential decay with increasing genome sizes. The functions, ATP binding (GO:0005524), GTP binding (GO:0005525), and DNA-directed RNA polymerase activity (GO:0003899), are likely required for organisms across life domains.
粗俗人
发表于 2025-3-26 02:50:15
http://reply.papertrans.cn/39/3820/381915/381915_26.png
esoteric
发表于 2025-3-26 08:07:45
Microarray Transposon Tracking for the Mapping of Conditionally Essential Genes in ,,wth conditions. With a fully saturated library, the absence of transposon insertions can be used as an indicator of a gene essential for the survival and growth for the conditions used for the mutant library.
Individual
发表于 2025-3-26 09:44:37
Identification of Essential Genes and Synthetic Lethal Gene Combinations in , K-12,io single-gene deletion library, we undertook the development of the ASKA single-gene deletion library carrying a different antibiotic resistance. In addition, we developed tools for identification of synthetic lethal gene combinations by systematic construction of double-gene knockout mutants. We introduce these methods herein.
Palate
发表于 2025-3-26 13:36:05
http://reply.papertrans.cn/39/3820/381915/381915_29.png
陶器
发表于 2025-3-26 20:44:50
Children, their Families and the Lawxtraction of genomic DNA, amplification and quantification of transposon insertions through next-generation deep sequencing are covered. Determining gene essentiality and statistical analysis on data collected are also discussed.