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Sample GSM5958596 Query DataSets for GSM5958596
Status Public on Jun 16, 2022
Title nonselect_library_replicate1_tile2
Sample type SRA
 
Source name Yeast cells
Organism synthetic construct
Characteristics host yeast strain: hxk1deltahxk2deltaglk1delta
selection: no
molecule subtype: plasmid
Growth protocol Following transformation, yeast cells were grown in SC-URA galactose until saturation. Cells were either pelleted and stored at -20C before plasmid DNA extraction to serve as the nonselect condition or used for selection. For selection of GCK activity, cells were grown on solid SC-URA 0.2% glucose for three days at 30C. After selection, cells were pelleted and stored at -20C prior to plasmid DNA extraction to serve as the post-selection samples (select).
Extracted molecule genomic DNA
Extraction protocol For each condition (select/nonselect, library/wt, replicate1/replicate2), 9 OD units of cells were used for plasmid DNA extraction using the ChargeSwitch Plasmid Yeast Mini kit (Invitrogen) according to the manufacturer's instructions.
The three regional libraries spanning the GCK sequence (aa 2-171, 172-337, 338-466) were constructed by pooled mutagenesis using NNK-degenerate oligos.
 
Library strategy OTHER
Library source genomic
Library selection other
Instrument model NextSeq 550
 
Description Amino acid positions 38-69
Data processing Library strategy: Tile-Seq
Libraries were sequenced on a NextSeq 550 instrument (Illumina) and base called using the instriment's Real Time Analysis software.
Sequencing reads were converted to fastq format and demultiplexed using BaseSpace Sequence Hub.
Reads were alligned and variants called using the TileSeq mutation count pipeline (https://github.com/RyogaLi/tileseq_mutcount) version 0.5.9
Variant calls from the TileSeq mutation count pipeline were then used for calling protein-level amino acid changes and for calculating the enrichment of variants using the TileSeqMave pipeline (https://github.com/jweile/tileseqMave) version 0.6.0.9000
reference sequence: sequence.txt on the series record contains the sequence used for read alignment.
 
Submission date Mar 17, 2022
Last update date Jun 16, 2022
Contact name Sarah Gersing
E-mail(s) sarah.gersing@bio.ku.dk
Organization name University of Copenhagen
Street address Ole Maaløes vej 5
City Copenhagen N
State/province -
ZIP/Postal code 2200
Country Denmark
 
Platform ID GPL27609
Series (1)
GSE198878 Multiplexed assessment of human glucokinase variant activity
Relations
BioSample SAMN26750764
SRA SRX14486701

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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