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. 2019 Oct 7;8:401. Originally published 2019 Apr 8. [Version 3] doi: 10.12688/f1000research.16734.3

Draft genome assembly and transcriptome sequencing of the golden algae Hydrurus foetidus (Chrysophyceae)

Jon Bråte 1,a, Janina Fuss 2, Shruti Mehrotra 1,3, Kjetill S Jakobsen 4, Dag Klaveness 3
PMCID: PMC6784874  PMID: 31632652

Version Changes

Revised. Amendments from Version 2

We have added Shruti Mehrotra as a co-author as she was responsible for culturing and isolation of genomic DNA for Illumina sequencing. We have also added a citation to her unpublished master thesis where this work was first described.

Abstract

Hydrurus foetidus is a freshwater chrysophyte alga. It thrives in cold rivers in polar and high alpine regions. It has several morphological traits reminiscent of single-celled eukaryotes, but can also form macroscopic thalli. Despite its ability to produce polyunsaturated fatty acids, its life under cold conditions and its variable morphology, very little is known about its genome and transcriptome. Here, we present an extensive set of next-generation sequencing data, including genomic short reads from Illumina sequencing and long reads from Nanopore sequencing, as well as full length cDNAs from PacBio IsoSeq sequencing and a small RNA dataset (smaller than 200 bp) sequenced with Illumina. The genome sequences were combined  to produce an assembly consisting of 5069 contigs, with a total assembly size of 171 Mb and a 77% BUSCO completeness. The new data generated here may contribute to a better understanding of the evolution and ecological roles of chrysophyte algae, as well as to resolve the branching patterns at a larger phylogenetic scale.

Keywords: Hydrurus foetidus, Chrysophyceae, golden algae, genome, transcriptome, Nanopore, PacBio

Introduction

Here, we present extensive genome sequencing data, including a hybrid assembly, as well as transcriptome data of mRNAs and small RNAs of the golden algae Hydrurus foetidus (Villars) Trevisan.

There has been considerable interest in the golden algae for many reasons: they are ecologically diverse, important as primary producers (phototrophs) in oligotrophic to dystrophic lakes ( Kristiansen, 2005; Nicholls & Wujek, 2015), some are also mixotrophs, phagotrophs or osmotrophs ( Kristiansen & Preisig, 2001; Pringsheim, 1963). The chrysophytes span a large range of feeding and nutrient uptake modes ( Kristiansen, 2005) and therefore play a significant role in aquatic food webs. Chrysophytes also make up a significant fraction of sequence reads and novel operational taxonomic units in clone libraries from freshwater environmental samples ( del Campo & Massana, 2011).

However, chrysophytes have also attracted considerable interest from an evolutionary point of view. They belong to the division (phylum) Heterokonta ( Cavalier-Smith, 1986) (Stramenopila according to Adl et al., 2019), an immensely diverse group of eukaryotes with many basal branches in the phylogeny still not resolved, despite numerous molecular phylogenetic studies, including multigene phylogenomics (e.g. Burki, 2014; Grossmann et al., 2016; Riisberg et al., 2009; Scoble & Cavalier-Smith, 2014). One reason for this is the presence of cryptic species and many groups with extremely similar morphology ( Grossmann et al., 2016). Another reason is the complex evolutionary history of the Heterokonta, including an elaborate plastid evolution (e.g. Kim et al., 2019) and heterotrophic lineages which have lost the plastids altogether ( Graupner et al., 2018; Pringsheim, 1963). The lack of genomic or transcriptomic data from many taxa, and even whole orders, which limits the power of multigene phylogenies ( Beisser et al., 2017), is yet another motivation for genomic and transcriptomic studies. However, recently, there has been a significant addition of transcriptomic data for chrysophyte taxa (e.g. Beisser et al., 2017; Graupner et al., 2018; Keeling et al., 2014; Kraus et al., 2019; Lie et al., 2017).

Hydrurus foetidus is not a typical representative of the golden algae. It is macroscopic and benthic (e.g. Klaveness et al., 2011; Rostafinski, 1882: Tab II, Szklarczyk, 1953), whereas most chrysophytes are microscopic single cells or colonial plankton ( Sandgren, 1988; Kristiansen, 2005). Furthermore, Hydrurus is native to polar, peri-glacial and alpine rivers in Norway and similar regions around the world (e.g. Klaveness, 2019; Rott et al., 2006; Rott & Schneider, 2014) and can only live in cold waters (2–10°C) ( Bursa, 1934; Kann, 1978). Members of the Hydrurus clade may cause colored snow and ice, and may be found on permanent ice sheets ( Klaveness et al., 2011; Lutz et al., 2018; Remias et al., 2013).

Hydrurus has a number of peculiar morphological characteristics relevant for understanding chrysophyte and heterokont evolution. Although it is multicellular, the cells in the thalli are not physically connected, and under some growth conditions the cells may slide away from each other in their wall-less polysaccharide tubes, or be released as single-celled swarmers ( Klaveness et al., 2011). Other characteristic features, which may be considered primitive for a thallose alga, are contractive vacuoles, often more than one in each cell ( Fott, 1959; Klaveness, 2019).

We have assembled a draft genome of Hydrurus foetidus using a combination of short-read Illumina sequencing and long-read Nanopore sequencing. The assembly consists of 5069 contigs yielding a total size of 171 Mb and a 77% BUSCO completeness. In addition to the deep genomic sequencing, we have also sequenced full-length poly(A) transcripts using PacBio IsoSeq, as well as sequencing the expressed small RNAs. This extensive dataset will be important, not only for studies of heterokont and chrysophyte evolution but also for elucidating the genetic mechanisms behind cold water adaptation, like the production of polyunsaturated fatty acids ( Klaveness, 2017) and the regulation of a complex multicellular lifestyle.

Materials and methods

Culturing of H. foetidus

The specimen of Hydrurus foetidus (Villars) Trevisan (strain G070301) used in this study was sampled from the river at the Finse Alpine Research Center (60°36' N. 07°30' E) in March 2007 and is currently kept in culture at University of Oslo. The photosynthetic H. foetidus was cultured at 4°C with a 14:10 hour light/dark cycle and kept in an adapted Guillard & Lorensen’s WC (Wright’s Chu) medium ( Guillard & Lorenzen, 1972) as described by Klaveness & Lindstrøm (2011). To prepare for DNA isolation, the growth of large thalli was promoted by repeated transfer of individual thalli into fresh culture media. Large thalli (0.5–1.0 g wet frozen weight) were collected by removal from the culture medium and immediate transfer to -80°C and storage until further processing. The culture will be deposited in a special culture collection, at the Fraunhofer Culture Collection of Cryophilic Algae (CCCryo).

Illumina sequencing of genomic DNA

Isolation of genomic DNA for Illumina sequencing was performed as part of an unpublished master project ( Mehrotra, 2018). Briefly, six individual thalli were used for the DNA isolation. DNA isolation was performed using the DNeasy Plant Mini Kit from Qiagen (Qiagen Inc., Valencia, CA, US). To ensure efficient lysis and homogenization of the external polysaccharide sheath, a few titanium beads were added to the frozen samples and the tubes were shaken using TissueLyser II machine (Qiagen Inc., Valencia, CA, US) for four minutes. After the addition of the lysis buffer and the RNase, tubes were placed in a thermomixer set at 65°C and 800 rpm with 20 second intervals for 30 mins. After adding Buffer AP2 to the lysate, the incubation was done on ice for 15 minutes to allow for better precipitation of the polysaccharides. Further, the extraction kit protocol was followed as is, until the second elution step. Here we reused the flow through from the previous step elution to avoid excessive dilution of the samples. Afterwards, the samples were de-salted and concentrated by ethanol precipitation and resuspension in 100 μl of Milli Q water. Finally, the samples were concentrated even further by pooling all the samples and freeze drying with a Leybold-Heraeus Lyovac GT2 (Leybold-Heraeus, Köln, Germany). The final sample had a concentration of 104 ng/μl and 260/280 ratio of 1.85 and 260/230 ratio of 1.47 as measured on a Nanodrop ND-1000 (ThermoFisher, MA, US).

The isolated and freeze-dried genomic DNA was sent to the Norwegian Sequencing Center (NSC) at the University of Oslo for library preparation and sequencing. Briefly, the sequencing library was made with the Illumina Truseq LT DNA kit (following the rapid mode protocol), with 600–700 bp fragment size and sequenced on two lanes of Illumina HiSeq 2500 with 250 bp paired-end reads ( Table 1).

Table 1. Overview of datasets produced in this study.

Dataset Description Accession
Hfoetidus_ACAGTG_L001_R1_001.fastq.gz
Hfoetidus_ACAGTG_L001_R1_001.fastq.gz		 Genomic DNA sequenced with Illumina HiSeq 2500. ERR2882522
Hfoetidus_ACAGTG_L002_R1_001.fastq.gz
Hfoetidus_ACAGTG_L002_R1_001.fastq.gz		 Genomic DNA sequenced with Illumina HiSeq 2500. ERR3188711
Hydrurus_nanopore_fastq_files.tar.gz Basecalled Oxford Nanopore reads ERR2887871
IsoSeq_1-2kb_polished_low_qv_consensus_isoforms.fastq.gz mRNA sequenced with PacBio SMRT RSII. ERR2882521
IsoSeq_1-2kb_polished_high_qv_consensus_isoforms.fastq.gz mRNA sequenced with PacBio SMRT RSII. ERR2869477
IsoSeq_2-3kb_polished_low_qv_consensus_isoforms.fastq.gz mRNA sequenced with PacBio SMRT RSII. ERR2869481
IsoSeq_2-3kb_polished_high_qv_consensus_isoforms.fastq.gz mRNA sequenced with PacBio SMRT RSII. ERR2869478
IsoSeq_3-6kb_polished_low_qv_consensus_isoforms.fastq.gz mRNA sequenced with PacBio SMRT RSII. ERR2869484
IsoSeq_3-6kb_polished_high_qv_consensus_isoforms.fastq.gz mRNA sequenced with PacBio SMRT RSII. ERR2869483
1-Hfo-miRNA_S6_R1_001.fastq.gz Small RNA sequenced with Illumina NextSeq 500. ERR2869485
pilon_round3.fasta.gz Draft genome assembly GCA_900617105.1
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Nanopore sequencing of genomic DNA

Genomic DNA was isolated from two thalli as described above, except that tissue lysis was done using MagNA Lyser Green Beads (Roche, Penzberg, Germany) and shaken for 15 sec at 4 m/sec and the incubation at 65°C was done for 10 min. In addition, the supernatant (after adding buffer AP2) was run through QiaShredder columns to further homogenize the lysate. The DNA was eluted (twice, but re-using the elution buffer) in 50 µl AE elution buffer. To further clean and concentrate the samples, the samples were pooled and cleaned using the Zymo DNA Clean & Concentrate kit (Zymo Research, CA, US). The sample was double-eluted (as before) in 50 µl kit provided elution buffer (DNA concentration 61.8 ng/μl, 260/280 ratio of 1.93 and 260/230 ratio 2.05 as measured on a Nanodrop).

DNA sequencing was done using the MinION (MIN-101B) sequencer, the R9.5 Flow Cell and following the SQK-LSK108 protocol (version GDE_9002_v108_revT_18Oct2016) (Oxford Nanopore, Oxford, UK). Approximately 1 µg of starting DNA was used and inspection of the DNA on a 0.7% agarose gel run at 30 volts from 18 hours showed that the majority of the DNA was between 20-30 kbp, but with a long tail of shorter fragments. The sequencing was run using the MinKNOW software (Oxford Nanopore, Oxford, UK; downloaded October 2017) on an iMac and stopped after 36 hours. Base-calling of the raw Nanopore sequence data was done using Albacore v.2.1.10 (Linux, Python 3.5 version; Oxford Nanopore, Oxford, UK) with default settings. The process was run on the Abel computing cluster at the University of Oslo.

PacBio transcriptome sequencing

Total RNA was isolated from one frozen thallus using Qiagen RNeasy Plant kit, including a QiaShredder column and lysis using MagNA lyser beads as described above, otherwise following the kit protocol. Isolated RNA was sent to NSC for library preparation and PacBio sequencing. Three size fractions (1-2 kbp, 2-3 kbp and 3-5 kbp) were prepared using the IsoSeq library preparation protocol (with selection of polyadenylated transcripts) and sequenced on RSII SMRT cells (Pacific Biosciences, CA, US) ( Table 1 and Table 2).

Table 2. Summary of the read numbers in the different file types of the IsoSeq data set.

Size fraction
Library < 1kb 1-2kb 2-3kb 3-4kb 4-5kb 5-6kb > 6kb
1-2kb_high 7310 31953 17 0 0 0 0
1-2kb_low 903 5908 170 110 89 39 80
2-3kb_high 596 2703 37399 217 443 147 0
2-3kb_low 78 586 7749 116 301 134 215
3-6kb_high 8 13 552 28621 4603 20 388
3-6kb_low 0 6 268 8830 1535 74 418
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The suffixes “_high” and “_low” refers to the high- and low-quality sequences produced by the IsoSeq sequencing. The data files have the following accession numbers: 1-2kb_high – ERR2869477; 1-2kb_low - ERR2882521; 2-3kb_high - ERR2869478; 2-3kb_low - ERR2869481; 3-6kb_high - ERR2869483; 3-6kb_low - ERR2869484.

Illumina small RNA sequencing

Small RNAs (below 200 bp) were isolated from a frozen thallus using the Sigma mirPremier kit (Sigma-Aldrich, MO, US) following the manufacturer’s instructions, but including lysis with MagNA beads as described above. The sample was sent to the NSC for library preparation and sequencing. Sequencing library (up to approx. 40 nt fragment size) was prepared and sequenced with Illumina NextSeq 500 as single-end 75 bp reads ( Table 1).

Draft genome assembly

The basecalled Nanopore reads were processed with Porechop v0.2.2 using default parameters to remove sequencing adapters. Next, the reads were filtered with Nanofilt v2.0.0 ( De Coster et al., 2018) to remove reads shorter than 500 bp and average quality below 9. The filtered reads were further error-corrected with LoRDEC v0.7 ( Salmela & Rivals, 2014) using the Illumina reads. First the Illumina reads were quality assessed by removing sequencing adapters and bases with an average quality below 20 (average score across 4 bases), in addition to leading and trailing bases with a quality below 20. This was done using Trimmomatic v0.36 ( Bolger et al., 2014). Then lordec-correct (options -k 21 -s 3) was run with the trimmed Illumina reads to correct the filtered Nanopore reads. Then the corrected reads were run through Canu v1.6 ( Koren et al., 2017) for further correction (canu -correct with genome Size set to 300 m) and trimming (canu -trim) before assembly (canu -assemble). The assembly was done with two different corrected error rates, 0.144 and 0.146. The two assemblies were almost identical, but the results from using the corrected error rate of 0.144 were used further because the total size was slightly larger and also had the largest contig. The Canu assembly was then polished using the trimmed Illumina reads (described above) by running three rounds of Pilon v1.22 ( Walker et al., 2014). The final genome assembly consisted of 5069 contigs with a total length of 171 183 409 nt. The N50 was 43,856 nt and the longest contig of 5,118,963 nt ( Table 3).

Table 3. Statistics of the Hydrurus foetidus draft genome assembly.

Number of
contigs > 1000 bp		 Largest contig Contig N50 Assembly size Estimated
genome size a 		Complete and fragmented
BUSCO orthologs b 		GC (%)
5069 5118963 bp 43856 bp 171 Mb 299.9 Mb 77.2% 45.4
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aThe genome size estimation was based on k-mer frequencies on the Illumina data.

bBUSCO was run against the Eukaryota dataset.

Data availability

All Hydrurus foetidus datasets produced in this study are available, study accession number PRJEB29405: https://identifiers.org/ena.embl/PRJEB29405.

Acknowledgements

We thank the Norwegian Sequencing Centre for all sequence library preparations and sequencing services.

Funding Statement

JB was funded by the Research Council of Norway (grant numbers: 213703 and 240284).

The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

[version 3; peer review: 2 approved]

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F1000Res. 2019 Oct 7. doi: 10.5256/f1000research.22969.r54753

Reviewer response for version 3

Daniela Beisser 1, Stephan Majda 1

The authors answered most of our comments to our satisfaction. Minor comments regarding the methods describing the BUSCO analysis (which version was used?) and genome size estimation (which tool and parameters e.g. k-mer size were used?) are still missing. Overall, we suggest to accept the manuscript.

We confirm that we have read this submission and believe that we have an appropriate level of expertise to confirm that it is of an acceptable scientific standard.

F1000Res. 2019 Aug 12. doi: 10.5256/f1000research.18291.r49312

Reviewer response for version 1

Blake T Hovde 1

Review of Draft Genomes: Draft genome assembly and transcriptome sequencing of the golden algae Hydrurus foetidus (Chrysophyceae):

This data note represents a significant contribution to the algal genomics research community in couple different ways. This project represents the first publicly available draft genome of a chrysophyte (golden algae) to date, making it a critical contribution to the study of this particular clade of algae and will be a much-utilized resource for other chrysophyte genome analyses as they emerge. Because this is the first representative of Chrysophyceae to be sequenced is will be a de facto resource, which leads to the next important contribution of the note – which is the importance of the modern sequencing technologies used in development of this genome and transcriptome assembly. The tools used are likely to be the gold-standard tools of de novo genome and transcriptome sequencing and assembly. The use of Pacific Biosciences “Isoseq” long read, full length transcriptome sequencing approach will allow this team to generate high quality gene annotations, a great advantage for a new reference such as this genome. Additionally, the use of long read technologies (either Nanopore or PacBio) will be used to generate higher quality genome assemblies with fewer, longer contigs and scaffolds.

While broad strokes are painted about the contribution of this draft genome to phylogenetic (or phylogenomic) analysis and the importance of the algae as primary producers it is unclear what additional analyses this team will be doing to utilize this genome assembly. Next steps may be to perform biosynthetic pathway analyses and phylogenetic analysis of the Chysophte class or higher level algal/protist analysis. It would be beneficial if the authors could point to some specific follow-ups.

I was unable to locate the genome assembly using accession number ERZ780628as listed in Table 1. Though, I was able to find the assembly under NCBI accession number: GCA_900617105.1

I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard.

F1000Res. 2019 Aug 29.
Jon Bråte 1

We thank the reviewer for the critical reading. We have updated the accession number to the genome assembly (now GCA_900617105.1) and this should work both on EBI and NCBI.

F1000Res. 2019 May 9. doi: 10.5256/f1000research.18291.r47028

Reviewer response for version 1

Daniela Beisser 1, Stephan Majda 1

Please find below the comments to the article “Draft genome assembly and transcriptome sequencing of the golden algae Hydrurus foetidus (Chrysophyceae)” by Jon Bråte, Janina Fuss, Kjetill S. Jakobsen and Dag Klaveness.

The authors present in the article draft genome data for the chrysophyte Hydrurus foetidus. H. foetidus was chosen because it is a special chrysophyte which is, in contrast to most other chrysophytes, macroscopic, but cells can slide apart under some growth conditions, benthic and thrives under cold conditions in polar and high alpine regions.

The genome was sequenced using Illumina and Nanopore sequencing, in addition mRNA reads sequenced with PacBio and small RNA reads sequenced with Illumina are provided. The genome was assembled in a hybrid approach, resulting in a length of 171 Mb and 5,069 contigs with a BUSCO completeness of 77%.

DNA extraction, sequencing and assembly generation are described in detail, but some information is missing, which is listed below.

Overall, the work is technically sound and should be indexed after minor corrections.

Minor comments:

 

  1. Abstract: “We combined this data with, to our knowledge, the first draft genome assembly of a chrysophyte algae”. The data is not combined with the draft genome, maybe it should be “We combined this data to create, to our knowledge, the first draft genome assembly of a chrysophyte algae”. Further, there are two draft genomes listed at JGI for Ochromonas and Paraphysomonas species ( https://genome.jgi.doe.gov/portal/OchCCMStandDraft_FD/OchCCMStandDraft_FD.info.html, https://genome.jgi.doe.gov/portal/ParimpEvaluation_FD/ParimpEvaluation_FD.info.html). They cannot be accessed without registration, but perhaps they should be cited.

  2. Abstract: “...belonging to the phylum Heterokonta.” Recent classification of Eukaryotes (Adl et al 2005, 2012, 2018) 1 , 2 , 3 place the Chrysophyceae into the Stramenopiles which themselves belong to the SAR supergroup. The current classification should be adapted.

  3. Abstract: An assembly of 171 Mb was obtained, is this size expected? Is there other data available which suggests this genome size? On the other hand, the k-mer based genome size estimation suggests a much larger genome.

  4. Introduction: “multiapproach assembly”, should better be described as hybrid assembly.

  5. Culturing of H. foetidus: The introduction mentions plastid reduction and heterotrophy in chrysophyte species. H. foetidus in called alga, so I assume it is phototrophic, but it would be good to state that somewhere explicitly. Otherwise one would wonder if the cultures were axenic.

  6. Concerning the sequencing: Was there quality control performed by the sequencing center (RIN values etc.) before sequencing? Which library preparation protocols were used for the different sequencing data? Was the RNA rRNA-depleted before sequencing? What was the average sequence quality before and after filtering? An overview table of all the sequencing data including quality and number of reads/yield should be added.

  7. Nanopore sequencing of genomic DNA: “Albacore v2.1.10 (Linux, Python 3.5 version)” Please provide a reference for Albacore. The information that it was run under Linux with Python 3.5 is probably not necessary.

  8. Next line: Table 1 is not the correct reference for the sentence.

  9. Table 2: It is not described in the text or caption what “_high” and “_low” means.

  10. Table 3: The genome size estimation based on k-mers and BUSCO are not described in the methods section. Maybe the GC content could also be added to the table.

We confirm that we have read this submission and believe that we have an appropriate level of expertise to confirm that it is of an acceptable scientific standard, however we have significant reservations, as outlined above.

References

  • 1. : The new higher level classification of eukaryotes with emphasis on the taxonomy of protists. J Eukaryot Microbiol.52(5) : 10.1111/j.1550-7408.2005.00053.x 399-451 10.1111/j.1550-7408.2005.00053.x [DOI] [PubMed] [Google Scholar]
  • 2. : The revised classification of eukaryotes. J Eukaryot Microbiol.2012;59(5) : 10.1111/j.1550-7408.2012.00644.x 429-93 10.1111/j.1550-7408.2012.00644.x [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3. : Revisions to the Classification, Nomenclature, and Diversity of Eukaryotes. J Eukaryot Microbiol.2019;66(1) : 10.1111/jeu.12691 4-119 10.1111/jeu.12691 [DOI] [PMC free article] [PubMed] [Google Scholar]
F1000Res. 2019 Aug 29.
Jon Bråte 1

We thank the reviewer for the critical reading. Here are our responses to the minor comments:

1. We have rephrased the sentence and it no longer states that we present the first chrysophyte draft genome assembly.

2. We have rephrased the first sentence of the abstract. And the first time Heterokonta now is mentioned in the introduction we have also added that Adl et al. uses Stramenopila and added the reference. However, we prefer the name Heterokonta as it has seniority to Stramenopila, and is still used by for instance Cavalier-Smith (e.g. Ruggiero et al. 2015; A Higher Level Classification of All Living Organisms. Plos One:  https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4418965/).

3. The k-mer estimation was done on the Illumina data alone. While the assembly was done on the Nanopore reads alone (after error correcting with the Illumina reads). Also, k-mer basted estimations of genome size can be inaccurate, especially since we know nothing about the ploidy level or the amount of genetic variation between chromosome copies. Therefore we don't think that this discrepancy is particularly large or surprising.

4. Corrected.

5. We have added a sentence explicitly mentioning that H. foetidus is photosynthetic to the methods section under the paragraph describing the culture procedure. 

6. The PacBio transcriptome sequencing was performed by selecting for polydenylated transcripts (information now added to the manuscript), and for the smallRNA sequencing the totalRNA was size fractionated to remove ribosomal RNA. Information about concentration, integrity and library preparation protocols have been added for the Illumina DNA sequencing under the "Illumina sequencing of genomic DNA" section. Information about concentration and integrity of the DNA for Nanopore sequencing has been added to the section "Nanopore sequencing of genomic DNA". In our opinion, there is not much added value in showing the average sequence quality before trimming/filtering of the different datasets because the various quality thresholds used for the DNA sequences used in the assembly is described. For the small RNA and the transcriptome data we have not performed any filtering or assembly and the raw data is provided.

7. There are different versions of Albacore for different versions of Python. So, we believe it is more specific to keep this information. Albacore is not published (and it is not developed any more) but we added a reference to Oxford Nanopore who developed the software.

8. Corrected.

9. The information has been added.

10. The information has been added.

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Data Availability Statement

    All Hydrurus foetidus datasets produced in this study are available, study accession number PRJEB29405: https://identifiers.org/ena.embl/PRJEB29405.

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