|
|
GEO help: Mouse over screen elements for information. |
|
Status |
Public on Jun 10, 2021 |
Title |
100% HEK293T [ZZ203-PP04-A09] |
Sample type |
SRA |
|
|
Source name |
HEK293T/CCRM-CEM mixture
|
Organism |
Homo sapiens |
Characteristics |
x: ZZ203-PP04-A09 sample_id: ZZ203-PP04-A09 panel: broad construct: directPCR instrument_type: NEXTSEQ expected_neg: 0 ngs_repset: 297 ngs_repnum: 1 ngs_prep: ZZ203 pcr_primer_plate: PP04 pcr_primer_well: A09 read_pattern: 2x38 pcr_plate_ignore: 2 pcr_well_ignore: A09 seq_instrument: nwgc-nextseq-20190617 index_1: i7297 barcode_1: ACTGTCCT index_2: i5297 barcode_2: ACAGACGT pcr_plate: ZZ203-PCR2 pcr_well: A09 primer_plate: PP04 primer_well: A09 dsp_date: 20190607 dsp_instrument: Beta7 slide_type: 293T CPA dsp_plate_id: Beta 7: 1011220607190 dsp_aoi_by_plate: 9 dsp_well: A09 dsp_aoi_by_slide: 9 aoi_size: 300 aoi_area: 70686 exp_repset: 105 exp_repnum: 2 dsp_repset: 138 dsp_repnum: 2 segment_type: solid sample_name: HEK293T--CCRF-CEM sample_type: mixed cell line notes: 100% HEK293T uniq_id: ZZ203-PP04-A09 hk_geo: 1172.753865 q3: 207.087822 neg_geomean_bkp: 39.41410197 neg_geomean_lkp: 23.07670986 hk_factor: 3.775923582 q3_factor: 3.178166015 neg_bkp_factor: 3.020789076 neg_lkp_factor: 3.046250965 area_pixels: 446469 mean_intensity_blue: 2132 mean_intensity_green: 364 mean_intensity_yellow: na mean_intensity_red: 386 mix1: HEK293T mix2: CCRF-CEM mixprop: 1 hkfactor: 8.260661912384 bgmean: 4.80693777242841 bg.lkp: 4.31122911123 bg.bkp: 5.30264643362682
|
Extracted molecule |
total RNA |
Extraction protocol |
Samples were incubated with DNA-oligo barcoded RNA-ISH probes which were conjugated with a UV-photocleavable linker following standard ISH protocols, along with flourescently labeled antibodies for visualization of morphological structures. Regions of interest within the tissue were illuminated with UV light and oligo barcodes were physically aspirated from the tissue and collected into microtiter plates by the GeoMx® Digital Spatial Profiler (DSP) platform. For more information about DSP protocols please see Merritt et al. Nature Biotech 2020 (doi: 10.1038/s41598-020-63539-x) Each collection of oligo tags from one well (representing an AOI from the tissue section) was indexed with i7xi5 unique dual indexes using GeoMx SeqCode primers with 18 cycles of PCR. After PCR, indexed AOIs were pooled and purified in two rounds of AMPure XP PCR purification using 1.2x bead:sample ratio.
|
|
|
Library strategy |
OTHER |
Library source |
transcriptomic |
Library selection |
other |
Instrument model |
NextSeq 550 |
|
|
Description |
photocleaved oligonucleotide barcodes Samples were pooled during library preparation and split across lanes. Individual FASTQ files were generated for each lane, forward & reverse primers. The Fastq files contain the same identifier as the sample name for aggregation
|
Data processing |
Library strategy: GeoMx-Seq Adapter trimming with trim galore, trimGaloreOpts = " --hardtrim5 26 --dont_gzip" If paired-end, merge overlapping R1 and R2 with flash2, flash2Opts = " -m 26 -e 26 -f 26 -s 1 -r 27" Extract UMIs in bowtie2, umiExtractOpts = " --bc-pattern=NNNNNNNNNNNNNN" Align RTS_IDs (probe barcodes) using bowtie2, bowtie2Opts = " --end-to-end -L 4 --trim5 0 --trim3 0 --norc" Deduplication using UMI-tools, umiDedupOpts = " --edit-distance-threshold=1" Genome_build: N/A, sequencing of synthetic tags and alignment to whitelist of RTS_IDs (probe barcodes) found in the config.ini output from the GeoMx DSP platform Supplementary_files_format_and_content: Digital Count Conversion (DCC) file format outputted from GeoMx NGS Pipeline, contains software versions, scan attributes, GeoMx NGS pipeline parameters and output metrics, Q30 scores, and list of deduplicated counts per RTS_ID (probe barcode) Supplementary_files_format_and_content: Values represented in the collapsed target counts tab are the geometric mean of the probes for a given, removing any targets flagged as outliers. Analyzed counts represent the upper quartile normalized collapsed counts across the study after removing QC flagged segments.
|
|
|
Submission date |
May 20, 2021 |
Last update date |
Jun 10, 2021 |
Contact name |
Patrick Danaher |
Organization name |
NanoString Technologies, Inc.
|
Street address |
530 Fairview Ave N
|
City |
Seattle |
State/province |
WA |
ZIP/Postal code |
98109 |
Country |
USA |
|
|
Platform ID |
GPL21697 |
Series (2) |
GSE174746 |
GeoMx Cancer Transcriptome Atlas (CTA) mRNA assay on an FFPE cell pellet array of mixed HEK293T and CCRF-CEM cell lines. |
GSE175927 |
GeoMx Cancer Transcriptome Atlas (CTA) mRNA assay |
|
Relations |
BioSample |
SAMN19284611 |
SRA |
SRX10947783 |
Supplementary data files not provided |
SRA Run Selector |
Raw data are available in SRA |
Processed data are available on Series record |
|
|
|
|
|