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Chromium Single Cell CNV Solution Product Sheet

Chromium Brochure

Chromium Single Cell Gene Expression Solution Brochure

Chromium Genome Sequencing Solution Brochure

Chromium Exome Sequencing Solution Brochure

Chromium de novo Assembly Solution Brochure

Chromium Single Cell Gene Expression Solution Product Sheet

Chromium Single Cell Immune Profiling Solution Product Sheet

Chromium Genome Sequencing Solution Product Sheet

Chromium Exome Sequencing Solution Product Sheet

Chromium de novo Assembly Solution Product Sheet

Transcriptional Profiling of 1.3 Million Brain Cells with the Chromium Single Cell 3’ Solution

Discover Genetic Heterogeneity in Cancer

Characterization of the Tumor Microenvironment

Chromium Structural Variant Analysis with Linked-Reads

Chromium Genome Solution and Long Ranger for HLA Analysis

Resolving Cell Types as a Function of Read Depth and Cell Number

Chromium™ Single Cell V(D)J Libraries – Sequencing Metrics for Illumina® NovaSeq®

Chromium™ Genome v2 Libraries – Sequencing Metrics for Illumina® Sequencers

Chromium™ Single Cell V(D)J Libraries – Sequencing Metrics for Illumina® Sequencers

Comparison between Bioanalyzer and Fragment Analyzer Traces for QC of Chromium™ Genome v2 Libraries

Sample Preparation Recommendations for the Chromium™ Genome Kit

Comparison between Bioanalyzer and TapeStation traces for QC of Chromium™ Genome Libraries

Target Enrichment Using Custom Baits With The Chromium™ Genome Reagent Kit

Instructions to Download and Process FASTQs of 1.3M Brain Cells

Base Composition of Sequencing Reads of Chromium™ Single Cell 3’ v2 Libraries

Instructions to Download and Process BAM files of 1.3 Million Brain Cells

Guidelines for Accurate Target Cell Counts Using 10x Genomics® Single Cell Solutions

Base Composition of Sequencing Reads of Chromium™ Single Cell V(D)J Libraries

Chromium™ Genome v2 Libraries – Gel Bead Oligo Primer Contamination Affects Sequencing & Application Performance

Assay Scheme and Configuration of Chromium™ Single Cell V(D)J Libraries

Assay Scheme and Configuration of Chromium™ Single Cell 3′ v2 Libraries

Chromium™ Genome Libraries – Sequencing Metrics for Illumina® NovaSeq®

Chromium™ Single Cell 3’ v2 Libraries – Sequencing Metrics for Illumina® NovaSeq®

Introduction to Linked-Read Technology for a More Comprehensive Genome & Exome Analysis

Single-stranded DNA Damage and its Effects on Chromium™ Genome Application Performance

SPRIselect:DNA Ratios Affect the Size Range of Library Fragments

QC of Chromium™ Genome v2 Libraries: Qualitative Evaluation Using Agilent Bioanalyzer

Chromium™ Single Cell 3’ v2 Libraries – Sequencing Performance on Illumina® NextSeq® 500 Flow Cells

Removal of Dead Cells from Single Cell Suspensions Improves Performance for 10x Genomics® Single Cell Applications

QC of Chromium™ Genome Libraries: Qualitative Evaluation Using Agilent Bioanalyzer

QC of Chromium™ Genome Libraries: Quantitative Evaluation Using qPCR

10x Barcode Continuity during Library Sequencing

Chromium™ Single Cell Applications – Guidelines for Optimal Sample Preparation

Importance of Cell Stock Concentration for Accurate Target Cell Recovery

Chromium™ Genome Application Performance as a Result of DNA Quality & Sequencing Depth

Chromium™ Single Cell 3’ v2 Libraries – Sequencing Metrics for Illumina® Sequencers

Assay Scheme and Configuration of Chromium™ Genome v2 Libraries

Deciphering the tumor microenvironment cell by cell

Characterizing Genomic Variation and Tumor Heterogeneity in Cancer

A Scalable Microfluidic Platform for Determining Cellular Heterogeneity by Copy Number Detection

Analyzing Infiltrating B Cell Populations in the Tumor Microenvironment Using Single Cell Transcriptomics

Identifying Genetic Variation and Cellular Heterogeneity with a Comprehensive Cancer Analysis Toolkit

Single cell transcriptomics for characterization of normal and diseased endodermal tissues

Dissecting the microenvironment of multiple tumors by transcriptional profiling and immune repertoire sequencing

Single cell transcriptomics for characterization of complex cellular systems

Full spectrum genome analysis with Linked-Read sequencing

How to determine the genome sequence of single insects

Copy Number Profiling of Thousands of Single Cells in Parallel

Assembly of individual chromosomes at megabase scale using 10x Linked-Reads

Resolving the full spectrum of human genetic variation using Linked-Reads