Welcome to the amplican package. This vignette will walk you through our main package usage with example MiSeq dataset. You will learn how to interpret results, create summary reports and plot deletions, insertions and mutations with our functions. This package, amplican, is created for fast and precise analysis of CRISPR experiments.

1 Introduction

amplican creates reports of deletions, insertions, frameshifts, cut rates and other metrics in knitable to HTML style. amplican uses many Bioconductor and CRAN packages, and is high level package with purpose to align your fastq samples and automate analysis across different experiments. amplican maintains elasticity through configuration file, which, with your fastq samples are the only requirements.

For those inpatient of you, who want to see an example of our whole pipeline analysis on attached example data look here. Below you will find the conceptual map of amplican.

Conceptual map of amplican.

Below you will find the amplicanConsensus rules. That allow you to understand how ampliCan treats unambiguous forward and reverse reads. Green color indicates events that will be accepted. When forward and reverse reads agree, their events are in the same place and span the same length, we will take forward read event as representative. In case when events from forward and reverse read don’t agree we select event from strand with higher alignment score. In situation where one of the reads is not spanning event in question we consider this event as real (as we don’t have other information). If both strands cover event in question, but one strand has no indel, amplicanConsensus will change behavior according to the strict parameter.

Consensus rules of ampliCan.

2 Configuration file

To successfully run our analysis it is mandatory to have a configuration file. Take a look at our example:

ID	Barcode	Forward_Reads	Reverse_Reads	Group	guideRNA	Forward_Primer	Reverse_Primer	Direction	Amplicon	Donor
ID_1	barcode_1	R1_001.fastq	R2_001.fastq	Betty	AGGTGGTCAGGGAACTGG	AAGCTGACGGCTAAATGA	AATTACACAAGCGCAAACACAC	0	aagctgacggctaaatgaaaaatgtcaaacatctgttccaggtgctgcgtatgccagggcagaggAGGTGGTCAGGGAACTGGtggaggtcactgggataccctttcttcccacaccaatggggaaaggagtcctgccagatgaccatcccaactgtgttgctgcagccagatccaggtgtgtttgcgcttgtgtaatt
ID_2	barcode_1	R1_001.fastq	R2_001.fastq	Tom	TGACCCTCTGCCAACACAAGGGG	TGACCAAACCTTCTTAAGGTGC	CTCTGCTGCAAAATGCAAGG	1	aaatactgtcttgtgaccaaaccttcttaaggtgctattttgataataaactttattgtgcttttgtagttgtgCCCCTTGTGTTGGCAGAGGGTCAgcagaccagtaagtcttctcaatttcttttatttatgtgtagtgataaaaaaatgttaaattaaaattaaatgtttttttttgccttgcattttgcagcagaggatgat
ID_3	barcode_2	R1_002.fastq	R2_002.fastq	Tom	AGGTGGTCAGGGAACTGG	AAGCTGACGGCTAAATGA	AATTACACAAGCGCAAACACAC	0	aagctgacggctaaatgaaaaatgtcaaacatctgttccaggtgctgcgtatgccagggcagaggAGGTGGTCAGGGAACTGGtggaggtcactgggataccctttcttcccacaccaatggggaaaggagtcctgccagatgaccatcccaactgtgttgctgcagccagatccaggtgtgtttgcgcttgtgtaatt
ID_4	barcode_2	R1_002.fastq	R2_002.fastq	Betty	GTCCCTGCAACATTAAAGGCCGG	GCTGGCAACATTCCTACCAGT	GAGCGCTGAGGCAGGATTAT	0	gctggcaacattcctaccagtaatttacgtaaaaaaatgctataaaatgtgtagctctccagtctaatgtaacttgtgcttgcattgtgtttacaggaaaccaGTCCCTGCAACATTAAAGGCCGGaagtctaagaactcacatcagcaggtgtcaagtgtgcatgaagagggtataatcctgcctcagcgctc
ID_5	barcode_2	R1_002.fastq	R2_002.fastq	Betty	GTCCCTGCAACATTAAAGGCCGG	ACTGGCAACATTCCTACCAGT	ACTGGCTGAGGCAGGATTAT	0	actggcaacattcctaccagtaatttacgtaaaaaaatgctataaaatgtgtagctctccagtctaatgtaacttgtgcttgcattgtgtttacaggaaaccaGTCCCTGCAACATTAAAGGCCGGaagtctaagaactcacatcagcaggtgtcaagtgtgcatgaagagggtataatcctgcctcagccagt	actggcaacattcctaccagtaatttacgtaaaaaaatgctataaaatgtgtagctctccagtctaatgtaacttgtgcttgcattgtgtttacaggaaaccaGTCCCTGCAACATTAAAAGCCGGaagtctaagaactcacatcagcaggtgtcaagtgtgcatgaagagggtataatcctgcctcagccagt

Configuration file should be a “,” delimited csv file with information about your experiments. You can find example config file path by running:

system.file("extdata", "config.csv", package = "amplican")

Columns of the config file:

ID - should be a unique identifier of your experiments
Barcode - use this to group experiments with the same barcode
Forward_Reads, Reverse_Reads - put names of your files in these fields, you can put here files compressed to .gz, we will unpack them for you
Group - use this field if you want to group ID by other criteria, here for instance we will group by person that performed experiment, on later stage it is possible to generate report with breakdown using this field
guideRNA - put your guideRNA in 5’ to 3’ fashion here, if he has to be reverse complemented to be found in the amplicon put “1” into Direction field, we will use this field to make sure your guideRNA is inside the amplicon and during plotting of the results
Forward_Primer, Reverse_Primer - make sure these primers are correct for each of your IDs, Forward_Primer should be found in the amplicon as is, on the left side of the guide, Reverse_Primer reverse complement should be found on the amplicon on the right side of the guide
Direction - here “0” means guide does not requires to be reverse complemented to be matched to the amplicon, “1” means it should be reverse complemented, this field is also used when plotting deletions, mismatches and insertions
Amplicon - insert amplicon sequence as lower case letters, by putting UPPER CASE letters you can specify expected cut site, you should specify at least one cut site, here for example we specify in uppercase letter PAM sequence of the corresponding guideRNA
Donor - insert donor template if you have designed HDR experiments or used base editors, otherwise leave empty, but keep the column. amplican will estimate HDR efficiency based on the events from aligning donor and amplicon sequences, donor and reads and reads and amplicon.

If you have only forward primers leave column Reverse_Primer empty, leave empty also the Reverse_Reads column. You can still use amplican like normal.

3 Default options

To run amplican with default options, along with generation of all posible reports you can use amplicanPipeline function. We have already attached results of the default amplican analysis (look at other vignettes) of the example dataset, but take a look below at how you can do that yourself. Be prepared to grab a coffe when running amplicanPipeline with knit_files = TRUE as this will take some time. You will understand it is worth waiting when reports will be ready.

# path to example config file
config <- system.file("extdata", "config.csv", package = "amplican")
# path to example fastq files
fastq_folder <- system.file("extdata", package = "amplican") 
# output folder, a full path
results_folder <- tempdir()  

#  run amplican
amplicanPipeline(config, fastq_folder, results_folder)

# results of the analysis can be found at
message(results_folder)

Take a look into “results_folder” folder. Here you can find .Rmd files that are our reports for example dataset. We already crafted .html versions and you can find them in the “reports” folder. Open one of the reports with your favourite browser now. To zoom on an image just open it in new window (right click -> open image in new tab).

amplicanPipeline just crafted very detailed reports for you, but this is not all, if you need something different e.g. different plot colours, just change the .Rmd file and knit it again. This way you have all the power over plotting.

4 Files created during analysis

4.1 barcode_reads_filters.csv

First step of our analysis is to filter out reads that are not complying with our default restrictions:

bad base quality - default minimum base quality is 0
bad average quality - default minimum average quality is 30
bad alphabet - by default we accept only reads with A,C,T,G bases

Barcode	experiment_count	read_count	bad_base_quality	bad_average_quality	bad_alphabet	filtered_read_count	unique_reads	unassigned_reads	assigned_reads
barcode_1	2	20	0	3	0	17	11	4	7
barcode_2	3	21	0	0	0	21	9	0	9

This table is also summarized in one of the reports. As you can see for our example dataset we have two barcodes, to which correspond 21 and 20 reads. Six reads are rejected for barcode_1 due to bad alphabet and bad average quality. Each of the barcodes has unique reads, which means forward and reverse reads are compacted when they are identical. There is 8 and 9 unique reads for each barcode. One read failed with assignment for barcode_1, you can see this read in the top unassgned reads for barcode report in human readable form. Normally you will probably see only half of your reads being assigned to the barcodes. Reads are assigned when for forward read we can find forward primer and for reverse read we can find reverse primer. Primers have to be perfectly matched. Nevertheless, there is option fastqreads = 0.5 which changes method of assigning reads to each IDs. With this option specified only one of the reads (forward or reverse) have to have primer perfectly matched. If you don’t have the reverse reads or you don’t want to use them you can use option fastqreads = 1, this option should be detectd autmatically, if you leave empty field Reverse_Primer in the config file.

4.2 config_summary.csv

config_summary.csv contains extended version of the config file. It should provide you additional look at raw numbers which we use for various plots in reports. Take a look at example extension:

ID	Barcode	Reads	Reads_Filtered	Reads_In	Reads_Del	Reads_Edited	Reads_Frameshifted
ID_1	barcode_1	7	6	0	6	6	2
ID_2	barcode_1	6	6	0	6	6	4
ID_3	barcode_2	9	8	1	7	8	1
ID_4	barcode_2	7	7	7	4	7	2
ID_5	barcode_2	5	5	0	0	2	0

During amplicanPipeline these columns are added to the config file:

Reads_Del, Reads_In, Reads_Edited - number of deletions, insertions or any of those two (mutations) overlapping with user specified UPPER CASE group in the amplicon (extended by the buffer), events are confirmed with the reverse strand when using paired-end reads, for more information check amplicanConsensus
Frameshifted - number of reads that have frameshift (insertions and deletions)
PRIMER_DIMER - number of reads that were classified as PRIMER DIMERs
Reads - number of reads assigned to this unique ID
Reads_Filtered - number of reads assigned to this unique ID with excusion of PRIMER DIMERs and Low Alignment Score reads

4.3 RunParameters.txt

File RunParameters.txt lists all options used for the analysis, this file you might find useful when reviewing analysis from the past where you forgot what kind of options you used. Other than that this file has no purpose.

# path to example RunParameters.txt
run_params <- system.file("extdata", "results", "RunParameters.txt", 
                          package = "amplican")
# show contents of the file
readLines(run_params)

##  [1] "Config file:         full/path/to/config/file/that/has/been/used.csv"                       
##  [2] "Average Quality:     30"                                                                    
##  [3] "Minimum Quality:     0"                                                                     
##  [4] "Filter N-reads:      FALSE"                                                                 
##  [5] "Batch size:          1e+07"                                                                 
##  [6] "Write Alignments:    txt"                                                                   
##  [7] "Fastq files Mode:    0"                                                                     
##  [8] "Gap Opening:         25"                                                                    
##  [9] "Gap Extension:       0"                                                                     
## [10] "Consensus:           TRUE"                                                                  
## [11] "Normalize:           guideRNA, Group"                                                       
## [12] "PRIMER DIMER buffer: 30"                                                                    
## [13] "Cut buffer: 5"                                                                              
## [14] "Scoring Matrix:"                                                                            
## [15] ",A,C,G,T,M,R,W,S,Y,K,V,H,D,B,N"                                                             
## [16] "A,5,-4,-4,-4,0.5,0.5,0.5,-4,-4,-4,-1,-1,-1,-4,-1.75"                                        
## [17] "C,-4,5,-4,-4,0.5,-4,-4,0.5,0.5,-4,-1,-1,-4,-1,-1.75"                                        
## [18] "G,-4,-4,5,-4,-4,0.5,-4,0.5,-4,0.5,-1,-4,-1,-1,-1.75"                                        
## [19] "T,-4,-4,-4,5,-4,-4,0.5,-4,0.5,0.5,-4,-1,-1,-1,-1.75"                                        
## [20] "M,0.5,0.5,-4,-4,0.5,-1.75,-1.75,-1.75,-1.75,-4,-1,-1,-2.5,-2.5,-1.75"                       
## [21] "R,0.5,-4,0.5,-4,-1.75,0.5,-1.75,-1.75,-4,-1.75,-1,-2.5,-1,-2.5,-1.75"                       
## [22] "W,0.5,-4,-4,0.5,-1.75,-1.75,0.5,-4,-1.75,-1.75,-2.5,-1,-1,-2.5,-1.75"                       
## [23] "S,-4,0.5,0.5,-4,-1.75,-1.75,-4,0.5,-1.75,-1.75,-1,-2.5,-2.5,-1,-1.75"                       
## [24] "Y,-4,0.5,-4,0.5,-1.75,-4,-1.75,-1.75,0.5,-1.75,-2.5,-1,-2.5,-1,-1.75"                       
## [25] "K,-4,-4,0.5,0.5,-4,-1.75,-1.75,-1.75,-1.75,0.5,-2.5,-2.5,-1,-1,-1.75"                       
## [26] "V,-1,-1,-1,-4,-1,-1,-2.5,-1,-2.5,-2.5,-1,-2,-2,-2,-1.75"                                    
## [27] "H,-1,-1,-4,-1,-1,-2.5,-1,-2.5,-1,-2.5,-2,-1,-2,-2,-1.75"                                    
## [28] "D,-1,-4,-1,-1,-2.5,-1,-1,-2.5,-2.5,-1,-2,-2,-1,-2,-1.75"                                    
## [29] "B,-4,-1,-1,-1,-2.5,-2.5,-2.5,-1,-1,-1,-2,-2,-2,-1,-1.75"                                    
## [30] "N,-1.75,-1.75,-1.75,-1.75,-1.75,-1.75,-1.75,-1.75,-1.75,-1.75,-1.75,-1.75,-1.75,-1.75,-1.75"

4.4 “alignments” folder

As name indicates it contains all alignments.

# path to the example alignments folder
system.file("extdata", "results", "alignments", package = "amplican")

In unassigned_reads.csv you can find detailed information about unassigned reads. In example dataset there is one unassigned read.

Take a look at the alignment events file which contains all the insertions, deletions, cuts and mutations. This file can be used in various ways. Examples you can find in .Rmd files we prepare using amplicanReport. These can be easily converted into GRanges and used for further analysis! Events are saved at three points of amplicanPipeline analysis. First file “raw_events.csv” contains all events directly extracted from aligned reads. After filtering PRIMER DIMER reads, removing events overlapping primers (alignment artifacts) and shifting events so that they are relative to the expected cut sites “events_filtered_shifted.csv” is saved. After normalization through amplicanNormalize “events_filtered_shifted_normalized.csv” is saved, probably it is the file you should use for further analysis.

seqnames	start	end	width	strand	originally	replacement	type	read_id	score	counts	readType	overlaps	consensus
ID_1	42	61	20	+		AAAAAAAAAAAAAAAAAAAA	insertion	1	597	3	FALSE	FALSE	TRUE
ID_1	46	65	20	+		AAAAAAAAAAAAAAAAAAAA	insertion	2	557	2	FALSE	FALSE	TRUE
ID_1	-24	41	66	+			deletion	1	597	3	FALSE	TRUE	TRUE
ID_1	-28	45	74	+			deletion	2	557	2	FALSE	TRUE	TRUE
ID_1	-32	51	84	+			deletion	4	532	1	FALSE	TRUE	TRUE
ID_1	-35	-35	1	+	A	G	mismatch	1	597	3	FALSE	FALSE	TRUE

Human readable alignments can be accesed using lookupAlignment function of AlignmentsExperimentSet object which contains all information after alignments from multiple experiments. Human readable format looks like this:

aln <- system.file("extdata", "results", "alignments", 
                   "AlignmentsExperimentSet.rds", 
                   package = "amplican")
aln <- readRDS(aln)
amplican::lookupAlignment(aln, ID = "ID_1") # will print most frequent alignment for ID_1

## ########################################
## # Forward read for ID ID_1 read_id 1
## # Program: Biostrings (version 2.64.0), a Bioconductor package
## # Rundate: Tue Apr 26 15:58:01 2022
## ########################################
## #=======================================
## #
## # Aligned sequences:
## # Forward read: P1
## # Amplicon sequence: S1
## # Matrix: NA
## # Gap_penalty: 25.0
## # Extend_penalty: 0.0
## #
## # Length: 219
## # Identity:     131/219 (59.8%)
## # Similarity:    NA/219 (NA%)
## # Gaps:          86/219 (39.3%)
## # Score: 597
## #
## #
## #=======================================
## 
## P1                 1 AAGCTGACGGCTAAATGAAAAATGTCAAACGTCTGTTCCAG---------     41
##                      |||||||||||||||||||||||||||||| ||||||||||         
## S1                 1 AAGCTGACGGCTAAATGAAAAATGTCAAACATCTGTTCCAGGTGCTGCGT     50
## 
## P1                42 --------------------------------------------------     41
##                                                                        
## S1                51 ATGCCAGGGCAGAGGAGGTGGTCAGGGAACTGGTGGAGGTCACTGGGATA    100
## 
## P1                42 -------AAAAAAAAAAAAAAAAAAAATTCCCACACCAATGGGGAAAGGA     84
##                                                 |||||||||||||||||||||||
## S1               101 CCCTTTC--------------------TTCCCACACCAATGGGGAAAGGA    130
## 
## P1                85 GTCCTGCCAGATGACCATCCCAACTGTGTTGCAGCAGCCAGATCCAGGTG    134
##                      |||||||||||||||||||||||||||||||| |||||||||||||||||
## S1               131 GTCCTGCCAGATGACCATCCCAACTGTGTTGCTGCAGCCAGATCCAGGTG    180
## 
## P1               135 TGTTTGCGCTTGTGTAATT    153
##                      |||||||||||||||||||
## S1               181 TGTTTGCGCTTGTGTAATT    199
## 
## 
## #---------------------------------------
## #---------------------------------------
## ########################################
## # Reverse read for ID ID_1 read_id 1
## # Program: Biostrings (version 2.64.0), a Bioconductor package
## # Rundate: Tue Apr 26 15:58:01 2022
## ########################################
## #=======================================
## #
## # Aligned sequences:
## # Reverse read: P1
## # Amplicon sequence: S1
## # Matrix: NA
## # Gap_penalty: 25.0
## # Extend_penalty: 0.0
## #
## # Length: 219
## # Identity:     131/219 (59.8%)
## # Similarity:    NA/219 (NA%)
## # Gaps:          86/219 (39.3%)
## # Score: 597
## #
## #
## #=======================================
## 
## P1                 1 AAGCTGACGGCTAAATGAAAAATGTCAAACGTCTGTTCCAG---------     41
##                      |||||||||||||||||||||||||||||| ||||||||||         
## S1                 1 AAGCTGACGGCTAAATGAAAAATGTCAAACATCTGTTCCAGGTGCTGCGT     50
## 
## P1                42 --------------------------------------------------     41
##                                                                        
## S1                51 ATGCCAGGGCAGAGGAGGTGGTCAGGGAACTGGTGGAGGTCACTGGGATA    100
## 
## P1                42 -------AAAAAAAAAAAAAAAAAAAATTCCCACACCAATGGGGAAAGGA     84
##                                                 |||||||||||||||||||||||
## S1               101 CCCTTTC--------------------TTCCCACACCAATGGGGAAAGGA    130
## 
## P1                85 GTCCTGCCAGATGACCATCCCAACTGTGTTGCAGCAGCCAGATCCAGGTG    134
##                      |||||||||||||||||||||||||||||||| |||||||||||||||||
## S1               131 GTCCTGCCAGATGACCATCCCAACTGTGTTGCTGCAGCCAGATCCAGGTG    180
## 
## P1               135 TGTTTGCGCTTGTGTAATT    153
##                      |||||||||||||||||||
## S1               181 TGTTTGCGCTTGTGTAATT    199
## 
## 
## #---------------------------------------
## #---------------------------------------

4.5 reports folder

Reports are automated for the convenience of the users. We provide 6 different reports. Reports are .Rmd files which can be easily crafted through rmarkdown::render(path_to_report) or by clicking Knit in Rstudio to make HTML version of the report. If you have run our example analysis, then you can open one of the reports with Rstudio and try knitting it now! Otherwise you can open one of already knitted example report in the vignettes.

5 Detailed analysis

5.1 Aligning reads

When you want to have more control over alignments and you need more advanced options use amplicanAlign. This function has many parameters which can be used to bend our pipeline to your needs. Read more about amplicanAlign on the help page ?amplican::amplicanAlign.

5.2 Normalization

Read more about normalization in the description of the ?amplican::amplicanNormalize or in FAQ. Just note that default setting of normalization threshold is 1%, if you notice in your mismatch plots that general level of noise (mismatches outside cut region) might be higher than that of 1%, you have to adjust threshold value to higher levels (min_freq input parameter). In case where you expect index hopping to occour, you can use either ?amplican::amplicanPipelineConservative or rise the min_freq above expected index hopping level.

5.3 Making reports

Reports are made for user convenience, they are powerful as they:

contain reproducible code
make plots ready for publication
show how to use results of our pipeline
are easy to share
allow quick, but detailed assessment of the data

We decided to separate reports into 6 different types. Function amplicanReport is made for automated report creation.

Types of report:

ID - Each of the IDs is treated separately, you get to see what kind of cuts, deletions, insertions and mismatches are being found for each of the IDs. example
Amplicon - We aggregate information about each unique amplicon, you will find here also plots for events found during alignment. example
Barcode - Grouped by Barcode, instead of the information about alignment events you can find here histograms explaining cut rates, frameshifts etc. example
Group - This field is for your convenience and allows you to group IDs by anything you want. In our example dataset we use this field to group experiments by the users. That will allow us to asses performance of our technicians. example
Guide - Unique guideRNAs are being summarized by boxplots showing cut rates across all experiments. example
Index - Has links to the other reports and can be treated as main summary. Contains overall statistics gathered during reads assesment. Can contain only barcode level information, but shows which parts of reads is being filtered. example

5.4 Plotting alignments events

We provide specialized plots for each type of the alignment events.

plot_mismatches - plots mismatches as stacked bar-plot over the amplicon, top plot is for the forward and bottom is for reverse reads
plot_deletions - plots deletions as arch-plot from the ggbio package
plot_insertions - each insertion is represented by triangle over the amplicon
plot_cuts - gathers cuts from each of the experiments and overlays multiple arch-plots on top of each other, useful when analyzing what kind of cuts were introduced in the amplicon
plot_variants - presents most frequent mutations with frameshift and codon information
plot_heterogeneity - shows a measure of read “uniqueness”

You can take a look at all these plots and how to make them in the example reports. There are also meta versions of above plots, that discard amplicon information and allow to overlay multiple different amplicons on top of each other eg. metaplot_deletions.

ampliCan Overview

26 April 2022

Package

Contents