Table 1 Genome statistics for the binned prokaryotic and eukaryotic populations and quality control statistics

From: Syntrophic linkage between predatory Carpediemonas and specific prokaryotic populations

Bin

Sequence size

No. contigs

% GC

Shortest contig

Mean sequence size

Longest contig

N50

Genome statistics for the binned prokaryotic and eukaryotic populations

Prolixibacteraceae

4 292 540

45

32.4

537

95 389.8

1448797

505417

Marinifilum

7 836 933

1089

37.8

601

7196.4

1053175

150714

Fusibacter

14 684 666

411

37.3

511

35 729.1

641269

190630

Fucophilus

4 491 245

124

54.3

627

36 219.7

3997856

3993360

Desulfovibrio

3 776 536

24

49.9

507

157 355.7

1377773

1119696

Desulfotalea

4 344 744

141

39.7

501

30 813.8

773452

260248

Desulfofaba

8 603 717

374

56.1

516

23 004.6

357581

54841

Carpediemonas

12 382 280

2326

58.6

500

5323.4

58509

9593

Bacillales

19 354 553

3057

32.3

500

6331.2

1002323

30666

Archaea

1 747 950

555

27

522

3149.5

61962

12541

Bin

Marker lineage

No. of genomes

No. of markers

No. of

marker sets

% Completeness

Contaminations

Strain heterogeneity

Quality control statistics

Prolixibacteraceae

Bacteroidetes

419

286

195

97.95

3.08

0

Marinifilum

Bacteroidetes

419

286

195

95.9

66.9

0.52

Fusibacter

Clostridia

446

196

110

100

206.57

4.98

Fucophilus

Verrucomicrobia

12

346

245

99.59

6.71

0

Desulfovibrio

Deltaproteobacteria

93

197

125

96.66

0

0

Desulfotalea

Deltaproteobacteria

93

197

125

99.6

6.78

7.32

Desulfofaba

Deltaproteobacteria

93

197

125

96

2.6

0

Bacilliales

Bacilli

821

250

136

96.69

449.99

3.3

Archaea

Archaea

207

149

107

72.9

4.67

14.29

  1. The marker lineages indicate the taxonomic rank of the lineage-specific marker set used to estimate quality control statistics. Genome completeness was estimated from the presence/absence of lineage specific marker genes. Contaminations were determined by the presence of multi-copy marker genes and the expected collocalization of these genes. Strain heterogeneity was determined by the number of multi-copy marker, which exceed a specified amino acid identity threshold. (See also Parks et al. (2015) for detailed explanation).