This protocol outlines the steps to prepare competent E. coli cells harboring the pSIM plasmid for lambda Red recombination using sacB as a counter-selectable marker. The process spans three days and includes streaking, culturing, induction of lambda Red proteins, cell preparation, transformation, and selection.
Shorthand | Strain | Notes | Paper | Table |
---|---|---|---|---|
Gallagher ... Manoil | 5075 | Most popular transposon library in Abau. References: Wang ... Mandel, Hauser | Gallagher et al (2015) | Presence means candidacy |
Geisinger ... Opijnen, Isberg | 17978 | Best coverage; Tn chemical genomics | Geisinger et al (2020) | Column F |
Wang ... Mandel, Hauser | 17978 | Poor coverage/sequencing/alignment; Tn-seq | Wang et al (2014) | [Tab A](https://journals-asm-org.ezproxy.library.wisc.edu/doi/suppl/10. |
The calculation of bottleneck size (
This method is an attempt to formalize the intial development from this GitHub repository, which is based on the methodologies from this Nature Methods paper.
- Add 200µL of DRUG A (100x) and 300µL of LB into the top-right well of a deep well plate, yielding a 40x concentration in a total volume of 500µL.
- Fill the rest of the wells in the top row with 250µL of LB.
- Perform a serial dilution across the top row by transferring 250µL sequentially from one well to the next.
- Discard 250µL from the penultimate well.
- Repeat steps 1-4 in the bottom-left well using DRUG B instead of DRUG A.
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#!/usr/bin/env bash | |
function get_headphones_index() { | |
echo $(pacmd list-cards | grep bluez_card -B1 | grep index | awk '{print $2}') | |
} | |
function get_headphones_mac_address() { | |
local temp=$(pacmd list-cards | grep bluez_card -C20 | grep 'device.string' | cut -d' ' -f 3) | |
temp="${temp%\"}" | |
temp="${temp#\"}" |
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= Arch Linux step-by-step installation = | |
= http://blog.fabio.mancinelli.me/2012/12/28/Arch_Linux_on_BTRFS.html = | |
== Boot the installation CD == | |
== Create partition == | |
cfdisk /dev/sda | |
* Create a partition with code 8300 (Linux) |