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6 protocols using 4200 tapestation d1000 screentape assay

1

Transcriptomic analysis via RNA-seq

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Total RNA was isolated using the Direct-zol RNA Miniprep Kit (Zymo). Libraries were prepared using the TruSeq Stranded Total RNA Library Prep Kit (Illumina), analyzed for insert size distribution using the 4200 TapeStation D1000 ScreenTape Assay (Agilent), and sequenced on Illumina NovaSeq 6000, yielding 100 million 100-bp paired-end reads. Sequences are deposited in GEO (GSE172221).
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2

RNA Isolation and Transcriptome Analysis

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The RNEasy kit (Qiagen) was used to isolate RNA from BMDM cells incubated 20 h in DMEM 1% DMSO ± 20 μM h18:0, and the TRIzol reagent (ThermoFisher) was used to isolate RNA from RAW 264.7 cells incubated 20 h in DMEM 1% DMSO ± 100 μM h18:0. RNA was quantified using the Quant-iT RiboGreen RNA assay (ThermoFisher) and quality checked by the 2100 Bioanalyzer RNA 6000 Nano assay (Agilent) or 4200 TapeStation High Sensitivity RNA ScreenTape assay (Agilent) prior to library generation. Libraries were prepared from total RNA with the TruSeq Stranded Total RNA Library Prep Kit according to the manufacturer’s instructions (Illumina, PN 20020599). Libraries were analyzed for insert size distribution using the 2100 BioAnalyzer High Sensitivity kit (Agilent), 4200 TapeStation D1000 ScreenTape assay (Agilent), or 5300 Fragment Analyzer NGS fragment kit (Agilent). Libraries were quantified using the Quant-iT PicoGreen ds DNA assay (ThermoFisher) or by low pass sequencing with a MiSeq nano kit (Illumina). Paired end 100 cycle sequencing was performed on a NovaSeq 6000 (Illumina).
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3

Bulk RNA-seq Library Preparation

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RNA was collected and purified using TRIzol according to the
manufacturer’s protocol. RNA-seq libraries were prepared with KAPA RNA
HyperPrep Kit with RiboErase (HMR) (KK8561) using standard protocols. Libraries
were analyzed for insert size distribution using the 2100 BioAnalyzer High
Sensitivity kit (Agilent), 4200 TapeStation D1000 ScreenTape assay (Agilent), or
5300 Fragment Analyzer NGS fragment kit (Agilent). RNA was sequenced at the
Genome Sequencing Facility at St. Jude Children’s Research Hospital on
Illumina HiSeq platform in paired-end mode with 100 bp per read.
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4

RNA Sequencing of Brain Tissue and Organoids

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Total RNA was isolated from brain tissue or organoids by using mirVana RNA isolation kit (ThermoFisher), quantified using the Quant-iT RiboGreen RNA assay (ThermoFisher), and quality checked by the 2100 Bioanalyzer RNA 6000 Nano assay (Agilent) or 4200 TapeStation High Sensitivity RNA ScreenTape assay (Agilent) prior to library generation. Libraries were prepared from total RNA with the TruSeq Stranded Total RNA Library Prep Kit according to the manufacturer’s instructions (Illumina, PN 20020599). Libraries were analyzed for insert-size distribution using the 2100 BioAnalyzer High Sensitivity kit (Agilent), 4200 TapeStation D1000 ScreenTape assay (Agilent), or 5300 Fragment Analyzer NGS fragment kit (Agilent). Libraries were quantified using the Quant-iT PicoGreen ds DNA assay (ThermoFisher) or by low-pass sequencing with a MiSeq nano kit (Illumina). Paired-end 100-cycle sequencing was performed on a NovaSeq 6000 (Illumina).
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5

RNA Immunoprecipitation and Sequencing Protocol

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Cells were treated with or without IFNβ for 48 hrs, harvested, and RIP conducted using the Magna RIP RNA-Binding Protein Immunoprecipitation Kit (Millipore) following the manufacturer’s instructions. Briefly, cell pellets were lysed in RIP lysis buffer, followed by incubation with RIP Buffer containing magnetic beads conjugated with Z-RNA or isotype control antibody at 4°C overnight. Samples were then incubated with proteinase K and immunoprecipitated RNAs were recovered by phenol:chloroform:isoamyl alcohol purification. RNA was quantified using the Quant-iT RiboGreen RNA assay (Thermo Fisher Scientific) and assessed for quality with the 2100 Bioanalyzer RNA 6000 Nano assay (Agilent) or 4200 TapeStation High Sensitivity RNA ScreenTape assay (Agilent) prior to library generation. Libraries were prepared from total RNA with the TruSeq Stranded Total RNA Library Prep Kit according to the manufacturer’s instructions (Illumina, PN 20020599). Libraries were analyzed for insert size distribution using the 2100 BioAnalyzer High Sensitivity kit (Agilent), 4200 TapeStation D1000 ScreenTape assay (Agilent), or 5300 Fragment Analyzer NGS fragment kit (Agilent). Libraries were quantified using the Quant-iT PicoGreen ds DNA assay (Thermo Fisher Scientific) or by low pass sequencing with a MiSeq nano kit (Illumina). Paired-end 150 cycle sequencing was performed on a NovaSeq 6000 (Illumina).
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6

RNA-seq Library Preparation with Spike-ins

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For RNA-seq experiments, ERCC RNA Spike-in Mix (Thermo Fisher, 4456740, 1 μL of 1:1,000 diluted spike-in mix per sample) and QIAseq miRNA Library QC Spike-in (Qiagen, 331535, 1 μL per sample) were added to 50 ng of total RNA per sample. Libraries were then prepared using the NEXTFLEX Combo-Seq mRNA/miRNA Kit (Perkin Elmer, NOVA-5139-02) per manufacturer’s instructions. Libraries were analyzed for insert size distribution using the 4200 TapeStation D1000 ScreenTape assay (Agilent). Libraries were quantified using the Quant-iT PicoGreen ds DNA assay (ThermoFisher). Paired end 100 cycle sequencing (cortex) or single end 50 cycle sequencing (hippocampus) was performed on a NovaSeq 6000 (Illumina). For paired end sequencing results (cortex), only read 1 data were used in downstream analyses, as the poly(A)-tail added during library preparation creates a poly(T)-stretch at the beginning of read 2 that reduces sequencing accuracy.
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